Canonical Allele Identifier: CA1327085369

Gene: BARD1

Linked Data

• dbSNP Id: rs1696491337
• gnomAD v4: 2-214809696-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809696C>T , CM000664.2:g.214809696C>T	GRCh38
NC_000002.11:g.215674420C>T , CM000664.1:g.215674420C>T	GRCh37
NC_000002.10:g.215382665C>T	NCBI36
NG_012047.2:g.5009G>A
NG_012047.3:g.5016G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.8:c.-127G>A	ENSP00000260947.4:n.-127G>A
ENST00000613374.4:c.-127G>A	ENSP00000484464.1:n.-127G>A
ENST00000613706.4:c.-127G>A	ENSP00000484976.1:n.-127G>A
ENST00000617164.4:c.-127G>A	ENSP00000480470.1:n.-127G>A
ENST00000619009.4:c.-127G>A	ENSP00000482293.1:n.-127G>A
NM_000465.3:c.-127G>A	NP_000456.2:n.-127G>A
NM_001282543.1:c.-127G>A	NP_001269472.1:n.-127G>A
NM_001282545.1:c.-127G>A	NP_001269474.1:n.-127G>A
NM_001282548.1:c.-127G>A	NP_001269477.1:n.-127G>A
NM_001282549.1:c.-127G>A	NP_001269478.1:n.-127G>A
NR_104212.1:n.16G>A
NR_104215.1:n.16G>A
NR_104216.1:n.16G>A
XM_011511568.1:c.-127G>A	XP_011509870.1:n.-127G>A