Canonical Allele Identifier: CA2662973051

Gene: BARD1

Linked Data

• gnomAD v4: 2-214809687-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809687A>C , CM000664.2:g.214809687A>C	GRCh38
NC_000002.11:g.215674411A>C , CM000664.1:g.215674411A>C	GRCh37
NC_000002.10:g.215382656A>C	NCBI36
NG_012047.2:g.5018T>G
NG_012047.3:g.5025T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.8:c.-118T>G	ENSP00000260947.4:n.-118T>G
ENST00000421162.1:c.-118T>G	ENSP00000392245.1:n.-118T>G
ENST00000613374.4:c.-118T>G	ENSP00000484464.1:n.-118T>G
ENST00000613706.4:c.-118T>G	ENSP00000484976.1:n.-118T>G
ENST00000617164.4:c.-118T>G	ENSP00000480470.1:n.-118T>G
ENST00000619009.4:c.-118T>G	ENSP00000482293.1:n.-118T>G
NM_000465.3:c.-118T>G	NP_000456.2:n.-118T>G
NM_001282543.1:c.-118T>G	NP_001269472.1:n.-118T>G
NM_001282545.1:c.-118T>G	NP_001269474.1:n.-118T>G
NM_001282548.1:c.-118T>G	NP_001269477.1:n.-118T>G
NM_001282549.1:c.-118T>G	NP_001269478.1:n.-118T>G
NR_104212.1:n.25T>G
NR_104215.1:n.25T>G
NR_104216.1:n.25T>G
XM_011511568.1:c.-118T>G	XP_011509870.1:n.-118T>G