Canonical Allele Identifier: CA350454622

Gene: BARD1

Linked Data

• ClinVar Variation Id: 823444
• ClinVar RCV Id: RCV001019693 ; RCV003607384
• dbSNP Id: rs1358719583
• gnomAD v2: 2-215645625-G-C
• gnomAD v4: 2-214780901-G-C
• MyVariant Identifiers: chr2:g.215645625G>C (hg19) ; chr2:g.214780901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780901G>C , CM000664.2:g.214780901G>C	GRCh38
NC_000002.11:g.215645625G>C , CM000664.1:g.215645625G>C	GRCh37
NC_000002.10:g.215353870G>C	NCBI36
NG_012047.2:g.33804C>G
NG_012047.3:g.33811C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.973C>G MANE Select	ENSP00000260947.4:p.His325Asp
ENST00000421162.2:c.215+16160C>G	ENSP00000392245.2:n.215+16160C>G
ENST00000613192.2:c.158+28511C>G	ENSP00000483275.2:n.158+28511C>G
ENST00000613374.5:c.159-28346C>G	ENSP00000484464.1:n.159-28346C>G
ENST00000613706.5:c.906+67C>G	ENSP00000484976.2:n.906+67C>G
ENST00000617164.5:c.916C>G	ENSP00000480470.1:p.His306Asp
ENST00000619009.5:c.364+11396C>G	ENSP00000482293.1:n.364+11396C>G
ENST00000650978.1:c.815C>G
ENST00000260947.8:c.973C>G	ENSP00000260947.4:p.His325Asp
ENST00000421162.1:c.215+16160C>G	ENSP00000392245.1:n.215+16160C>G
ENST00000455743.5:c.*593C>G	ENSP00000412186.1:n.*593C>G
ENST00000471787.1:n.868C>G
ENST00000613192.1:c.73+28511C>G	ENSP00000483275.1:n.73+28511C>G
ENST00000613374.4:c.159-28346C>G	ENSP00000484464.1:n.159-28346C>G
ENST00000613706.4:c.215+16160C>G	ENSP00000484976.1:n.215+16160C>G
ENST00000617164.4:c.916C>G	ENSP00000480470.1:p.His306Asp
ENST00000619009.4:c.364+11396C>G	ENSP00000482293.1:n.364+11396C>G
ENST00000620057.4:c.364+11396C>G	ENSP00000481988.1:n.364+11396C>G
NM_000465.3:c.973C>G	NP_000456.2:p.His325Asp
NM_001282543.1:c.916C>G	NP_001269472.1:p.His306Asp
NM_001282545.1:c.215+16160C>G	NP_001269474.1:n.215+16160C>G
NM_001282548.1:c.159-28346C>G	NP_001269477.1:n.159-28346C>G
NM_001282549.1:c.364+11396C>G	NP_001269478.1:n.364+11396C>G
NR_104212.1:n.966C>G
NR_104215.1:n.909C>G
NR_104216.1:n.506+11396C>G
XM_011511567.1:c.919C>G	XP_011509869.1:p.His307Asp
XM_011511568.1:c.973C>G	XP_011509870.1:p.His325Asp
XM_017004613.1:c.1072C>G	XP_016860102.1:p.His358Asp
XM_017004614.1:c.1072C>G	XP_016860103.1:p.His358Asp
XR_002959322.1:n.1163C>G
NM_000465.4:c.973C>G MANE Select	NP_000456.2:p.His325Asp
NM_001282543.2:c.916C>G	NP_001269472.1:p.His306Asp
NM_001282545.2:c.215+16160C>G	NP_001269474.1:n.215+16160C>G
NM_001282548.2:c.159-28346C>G	NP_001269477.1:n.159-28346C>G
NM_001282549.2:c.364+11396C>G	NP_001269478.1:n.364+11396C>G
NR_104212.2:n.938C>G
NR_104215.2:n.881C>G
NR_104216.2:n.478+11396C>G