Canonical Allele Identifier: CA2904385

Gene: GRXCR1

Linked Data

• dbSNP Id: rs751742351
• ExAC: 4:42964867 A / G
• gnomAD v2: 4-42964867-A-G
• gnomAD v3: 4-42962850-A-G
• gnomAD v4: 4-42962850-A-G
• MyVariant Identifiers: chr4:g.42964867A>G (hg19) ; chr4:g.42962850A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962850A>G , CM000666.2:g.42962850A>G	GRCh38
NC_000004.11:g.42964867A>G , CM000666.1:g.42964867A>G	GRCh37
NC_000004.10:g.42659624A>G	NCBI36
NG_027718.1:g.74585A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.385-42A>G MANE Select	ENSP00000382670.2:n.385-42A>G
ENST00000399770.2:c.385-42A>G	ENSP00000382670.2:n.385-42A>G
NM_001080476.2:c.385-42A>G	NP_001073945.1:n.385-42A>G
XM_011513691.1:c.22-42A>G	XP_011511993.1:n.22-42A>G
NM_001080476.3:c.385-42A>G MANE Select	NP_001073945.1:n.385-42A>G