Canonical Allele Identifier: CA96311669

Gene: GRXCR1

Linked Data

• dbSNP Id: rs547224307
• gnomAD v2: 4-42964830-C-G
• gnomAD v3: 4-42962813-C-G
• gnomAD v4: 4-42962813-C-G
• MyVariant Identifiers: chr4:g.42964830C>G (hg19) ; chr4:g.42962813C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962813C>G , CM000666.2:g.42962813C>G	GRCh38
NC_000004.11:g.42964830C>G , CM000666.1:g.42964830C>G	GRCh37
NC_000004.10:g.42659587C>G	NCBI36
NG_027718.1:g.74548C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.385-79C>G MANE Select	ENSP00000382670.2:n.385-79C>G
ENST00000399770.2:c.385-79C>G	ENSP00000382670.2:n.385-79C>G
NM_001080476.2:c.385-79C>G	NP_001073945.1:n.385-79C>G
XM_011513691.1:c.22-79C>G	XP_011511993.1:n.22-79C>G
NM_001080476.3:c.385-79C>G MANE Select	NP_001073945.1:n.385-79C>G