Canonical Allele Identifier: CA356792203
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42962946-C-A
MyVariant Identifiers: chr4:g.42964963C>A (hg19) chr4:g.42962946C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962946C>A , CM000666.2:g.42962946C>A GRCh38
NC_000004.11:g.42964963C>A , CM000666.1:g.42964963C>A GRCh37
NC_000004.10:g.42659720C>A NCBI36
NG_027718.1:g.74681C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.439C>A MANE Select ENSP00000382670.2:p.Arg147Ser
ENST00000399770.2:c.439C>A ENSP00000382670.2:p.Arg147Ser
NM_001080476.2:c.439C>A NP_001073945.1:p.Arg147Ser
XM_011513691.1:c.76C>A XP_011511993.1:p.Arg26Ser
NM_001080476.3:c.439C>A MANE Select NP_001073945.1:p.Arg147Ser
Search 100 bp 5'
Search 100 bp 3'