Canonical Allele Identifier: CA1061625423

Gene: GRXCR1

Linked Data

• dbSNP Id: rs1748167580
• gnomAD v3: 4-42963178-A-G
• gnomAD v4: 4-42963178-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963178A>G , CM000666.2:g.42963178A>G	GRCh38
NC_000004.11:g.42965195A>G , CM000666.1:g.42965195A>G	GRCh37
NC_000004.10:g.42659952A>G	NCBI36
NG_027718.1:g.74913A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.627+44A>G MANE Select	ENSP00000382670.2:n.627+44A>G
ENST00000399770.2:c.627+44A>G	ENSP00000382670.2:n.627+44A>G
NM_001080476.2:c.627+44A>G	NP_001073945.1:n.627+44A>G
XM_011513691.1:c.264+44A>G	XP_011511993.1:n.264+44A>G
NM_001080476.3:c.627+44A>G MANE Select	NP_001073945.1:n.627+44A>G