Canonical Allele Identifier: CA356792095
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1437816903
gnomAD v4: 4-42962892-C-T
COSMIC: COSM5515967
MyVariant Identifiers: chr4:g.42964909C>T (hg19) chr4:g.42962892C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962892C>T , CM000666.2:g.42962892C>T GRCh38
NC_000004.11:g.42964909C>T , CM000666.1:g.42964909C>T GRCh37
NC_000004.10:g.42659666C>T NCBI36
NG_027718.1:g.74627C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385C>T MANE Select ENSP00000382670.2:p.Gln129Ter
ENST00000399770.2:c.385C>T ENSP00000382670.2:p.Gln129Ter
NM_001080476.2:c.385C>T NP_001073945.1:p.Gln129Ter
XM_011513691.1:c.22C>T XP_011511993.1:p.Gln8Ter
NM_001080476.3:c.385C>T MANE Select NP_001073945.1:p.Gln129Ter
Search 100 bp 5'
Search 100 bp 3'