Canonical Allele Identifier: CA439191537
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42962954-C-G
MyVariant Identifiers: chr4:g.42964971C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962954C>G , CM000666.2:g.42962954C>G GRCh38
NC_000004.11:g.42964971C>G , CM000666.1:g.42964971C>G GRCh37
NC_000004.10:g.42659728C>G NCBI36
NG_027718.1:g.74689C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.447C>G MANE Select ENSP00000382670.2:p.Val149=
ENST00000399770.2:c.447C>G ENSP00000382670.2:p.Val149=
NM_001080476.2:c.447C>G NP_001073945.1:p.Val149=
XM_011513691.1:c.84C>G XP_011511993.1:p.Val28=
NM_001080476.3:c.447C>G MANE Select NP_001073945.1:p.Val149=
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