Canonical Allele Identifier: CA431148666
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 922064
ClinVar RCV Id: RCV001181912
dbSNP Id: rs770753803
MyVariant Identifiers: chr2:g.215674246G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214809522G>C , CM000664.2:g.214809522G>C GRCh38
NC_000002.11:g.215674246G>C , CM000664.1:g.215674246G>C GRCh37
NC_000002.10:g.215382491G>C NCBI36
NG_012047.2:g.5183C>G
NG_012047.3:g.5190C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.48C>G MANE Select ENSP00000260947.4:p.Ser16=
ENST00000421162.2:c.48C>G ENSP00000392245.2:p.Ser16=
ENST00000613192.2:c.48C>G ENSP00000483275.2:p.Ser16=
ENST00000613374.5:c.48C>G ENSP00000484464.1:p.Ser16=
ENST00000613706.5:c.48C>G ENSP00000484976.2:p.Ser16=
ENST00000617164.5:c.48C>G ENSP00000480470.1:p.Ser16=
ENST00000619009.5:c.48C>G ENSP00000482293.1:p.Ser16=
ENST00000260947.8:c.48C>G ENSP00000260947.4:p.Ser16=
ENST00000421162.1:c.48C>G ENSP00000392245.1:p.Ser16=
ENST00000455743.5:c.48C>G ENSP00000412186.1:p.Ser16=
ENST00000471787.1:n.149C>G
ENST00000479904.1:n.139C>G
ENST00000613192.1:c.-38C>G ENSP00000483275.1:n.-38C>G
ENST00000613374.4:c.48C>G ENSP00000484464.1:p.Ser16=
ENST00000613706.4:c.48C>G ENSP00000484976.1:p.Ser16=
ENST00000617164.4:c.48C>G ENSP00000480470.1:p.Ser16=
ENST00000619009.4:c.48C>G ENSP00000482293.1:p.Ser16=
ENST00000620057.4:c.48C>G ENSP00000481988.1:p.Ser16=
NM_000465.3:c.48C>G NP_000456.2:p.Ser16=
NM_001282543.1:c.48C>G NP_001269472.1:p.Ser16=
NM_001282545.1:c.48C>G NP_001269474.1:p.Ser16=
NM_001282548.1:c.48C>G NP_001269477.1:p.Ser16=
NM_001282549.1:c.48C>G NP_001269478.1:p.Ser16=
NR_104212.1:n.190C>G
NR_104215.1:n.190C>G
NR_104216.1:n.190C>G
XM_011511568.1:c.48C>G XP_011509870.1:p.Ser16=
XM_017004613.1:c.48C>G XP_016860102.1:p.Ser16=
XM_017004614.1:c.48C>G XP_016860103.1:p.Ser16=
XR_002959322.1:n.139C>G
NM_000465.4:c.48C>G MANE Select NP_000456.2:p.Ser16=
NM_001282543.2:c.48C>G NP_001269472.1:p.Ser16=
NM_001282545.2:c.48C>G NP_001269474.1:p.Ser16=
NM_001282548.2:c.48C>G NP_001269477.1:p.Ser16=
NM_001282549.2:c.48C>G NP_001269478.1:p.Ser16=
NR_104212.2:n.162C>G
NR_104215.2:n.162C>G
NR_104216.2:n.162C>G