Canonical Allele Identifier: CA96311689
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs777967428
gnomAD v2: 4-42965210-C-A
gnomAD v3: 4-42963193-C-A
gnomAD v4: 4-42963193-C-A
MyVariant Identifiers: chr4:g.42965210C>A (hg19) chr4:g.42963193C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963193C>A , CM000666.2:g.42963193C>A GRCh38
NC_000004.11:g.42965210C>A , CM000666.1:g.42965210C>A GRCh37
NC_000004.10:g.42659967C>A NCBI36
NG_027718.1:g.74928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+59C>A MANE Select ENSP00000382670.2:n.627+59C>A
ENST00000399770.2:c.627+59C>A ENSP00000382670.2:n.627+59C>A
NM_001080476.2:c.627+59C>A NP_001073945.1:n.627+59C>A
XM_011513691.1:c.264+59C>A XP_011511993.1:n.264+59C>A
NM_001080476.3:c.627+59C>A MANE Select NP_001073945.1:n.627+59C>A
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