Canonical Allele Identifier: CA2904402
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs142351714
ExAC: 4:42964964 G / C
gnomAD v2: 4-42964964-G-C
gnomAD v4: 4-42962947-G-C
MyVariant Identifiers: chr4:g.42964964G>C (hg19) chr4:g.42962947G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962947G>C , CM000666.2:g.42962947G>C GRCh38
NC_000004.11:g.42964964G>C , CM000666.1:g.42964964G>C GRCh37
NC_000004.10:g.42659721G>C NCBI36
NG_027718.1:g.74682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.440G>C MANE Select ENSP00000382670.2:p.Arg147Pro
ENST00000399770.2:c.440G>C ENSP00000382670.2:p.Arg147Pro
NM_001080476.2:c.440G>C NP_001073945.1:p.Arg147Pro
XM_011513691.1:c.77G>C XP_011511993.1:p.Arg26Pro
NM_001080476.3:c.440G>C MANE Select NP_001073945.1:p.Arg147Pro
Search 100 bp 5'
Search 100 bp 3'