Canonical Allele Identifier: CA356792581
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748165188
MyVariant Identifiers: chr4:g.42965145C>G (hg19) chr4:g.42963128C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963128C>G , CM000666.2:g.42963128C>G GRCh38
NC_000004.11:g.42965145C>G , CM000666.1:g.42965145C>G GRCh37
NC_000004.10:g.42659902C>G NCBI36
NG_027718.1:g.74863C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.621C>G MANE Select ENSP00000382670.2:p.Tyr207Ter
ENST00000399770.2:c.621C>G ENSP00000382670.2:p.Tyr207Ter
NM_001080476.2:c.621C>G NP_001073945.1:p.Tyr207Ter
XM_011513691.1:c.258C>G XP_011511993.1:p.Tyr86Ter
NM_001080476.3:c.621C>G MANE Select NP_001073945.1:p.Tyr207Ter
Search 100 bp 5'
Search 100 bp 3'