Canonical Allele Identifier: CA96311704
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs371446040
gnomAD v2: 4-42965324-G-A
gnomAD v3: 4-42963307-G-A
gnomAD v4: 4-42963307-G-A
MyVariant Identifiers: chr4:g.42965324G>A (hg19) chr4:g.42963307G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963307G>A , CM000666.2:g.42963307G>A GRCh38
NC_000004.11:g.42965324G>A , CM000666.1:g.42965324G>A GRCh37
NC_000004.10:g.42660081G>A NCBI36
NG_027718.1:g.75042G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+173G>A MANE Select ENSP00000382670.2:n.627+173G>A
ENST00000399770.2:c.627+173G>A ENSP00000382670.2:n.627+173G>A
NM_001080476.2:c.627+173G>A NP_001073945.1:n.627+173G>A
XM_011513691.1:c.264+173G>A XP_011511993.1:n.264+173G>A
NM_001080476.3:c.627+173G>A MANE Select NP_001073945.1:n.627+173G>A
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