Canonical Allele Identifier: CA439191464
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42964914A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962897A>T , CM000666.2:g.42962897A>T GRCh38
NC_000004.11:g.42964914A>T , CM000666.1:g.42964914A>T GRCh37
NC_000004.10:g.42659671A>T NCBI36
NG_027718.1:g.74632A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.390A>T MANE Select ENSP00000382670.2:p.Pro130=
ENST00000399770.2:c.390A>T ENSP00000382670.2:p.Pro130=
NM_001080476.2:c.390A>T NP_001073945.1:p.Pro130=
XM_011513691.1:c.27A>T XP_011511993.1:p.Pro9=
NM_001080476.3:c.390A>T MANE Select NP_001073945.1:p.Pro130=
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