Canonical Allele Identifier: CA356791502
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42895584A>G (hg19) chr4:g.42893567A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893567A>G , CM000666.2:g.42893567A>G GRCh38
NC_000004.11:g.42895584A>G , CM000666.1:g.42895584A>G GRCh37
NC_000004.10:g.42590341A>G NCBI36
NG_027718.1:g.5302A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.301A>G MANE Select ENSP00000382670.2:p.Ser101Gly
ENST00000399770.2:c.301A>G ENSP00000382670.2:p.Ser101Gly
NM_001080476.2:c.301A>G NP_001073945.1:p.Ser101Gly
NM_001080476.3:c.301A>G MANE Select NP_001073945.1:p.Ser101Gly
Search 100 bp 5'
Search 100 bp 3'