Canonical Allele Identifier: CA439191505
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1466002148
gnomAD v2: 4-42964947-T-A
gnomAD v4: 4-42962930-T-A
MyVariant Identifiers: chr4:g.42964947T>A (hg19) chr4:g.42962930T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962930T>A , CM000666.2:g.42962930T>A GRCh38
NC_000004.11:g.42964947T>A , CM000666.1:g.42964947T>A GRCh37
NC_000004.10:g.42659704T>A NCBI36
NG_027718.1:g.74665T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.423T>A MANE Select ENSP00000382670.2:p.Ile141=
ENST00000399770.2:c.423T>A ENSP00000382670.2:p.Ile141=
NM_001080476.2:c.423T>A NP_001073945.1:p.Ile141=
XM_011513691.1:c.60T>A XP_011511993.1:p.Ile20=
NM_001080476.3:c.423T>A MANE Select NP_001073945.1:p.Ile141=
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