Canonical Allele Identifier: CA356792408
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42963045-G-A
MyVariant Identifiers: chr4:g.42965062G>A (hg19) chr4:g.42963045G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963045G>A , CM000666.2:g.42963045G>A GRCh38
NC_000004.11:g.42965062G>A , CM000666.1:g.42965062G>A GRCh37
NC_000004.10:g.42659819G>A NCBI36
NG_027718.1:g.74780G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.538G>A MANE Select ENSP00000382670.2:p.Glu180Lys
ENST00000399770.2:c.538G>A ENSP00000382670.2:p.Glu180Lys
NM_001080476.2:c.538G>A NP_001073945.1:p.Glu180Lys
XM_011513691.1:c.175G>A XP_011511993.1:p.Glu59Lys
NM_001080476.3:c.538G>A MANE Select NP_001073945.1:p.Glu180Lys
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