Canonical Allele Identifier: CA580950557

Gene: HR

Linked Data

• dbSNP Id: rs774240157
• gnomAD v2: 8-21981131-C-G
• gnomAD v3: 8-22123618-C-G
• gnomAD v4: 8-22123618-C-G
• MyVariant Identifiers: chr8:g.21981131C>G (hg19) ; chr8:g.22123618C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123618C>G , CM000670.2:g.22123618C>G	GRCh38
NC_000008.10:g.21981131C>G , CM000670.1:g.21981131C>G	GRCh37
NC_000008.9:g.22037076C>G	NCBI36
NG_008166.1:g.11900G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381418.9:c.1915+31G>C MANE Select	ENSP00000370826.4:n.1915+31G>C
ENST00000680789.1:c.1915+31G>C	ENSP00000505181.1:n.1915+31G>C
ENST00000312841.9:c.1915+31G>C	ENSP00000326765.8:n.1915+31G>C
ENST00000381418.8:c.1915+31G>C	ENSP00000370826.4:n.1915+31G>C
NM_005144.4:c.1915+31G>C	NP_005135.2:n.1915+31G>C
NM_018411.4:c.1915+31G>C	NP_060881.2:n.1915+31G>C
XM_005273569.1:c.1918+31G>C	XP_005273626.1:n.1918+31G>C
XM_006716367.1:c.1918+31G>C	XP_006716430.1:n.1918+31G>C
XM_005273569.2:c.1918+31G>C	XP_005273626.1:n.1918+31G>C
XM_006716367.2:c.1918+31G>C	XP_006716430.1:n.1918+31G>C
NM_005144.5:c.1915+31G>C MANE Select	NP_005135.2:n.1915+31G>C