Canonical Allele Identifier: CA10621112
Gene: GRXCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 348826
ClinVar RCV Id: RCV000300716 RCV001653675
dbSNP Id: rs4861050
gnomAD v2: 4-43032612-G-A
gnomAD v3: 4-43030595-G-A
gnomAD v4: 4-43030595-G-A
MyVariant Identifiers: chr4:g.43032612G>A (hg19) chr4:g.43030595G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030595G>A , CM000666.2:g.43030595G>A GRCh38
NC_000004.11:g.43032612G>A , CM000666.1:g.43032612G>A GRCh37
NC_000004.10:g.42727369G>A NCBI36
NG_027718.1:g.142330G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.*55G>A MANE Select ENSP00000382670.2:n.*55G>A
ENST00000399770.2:c.928G>A ENSP00000382670.2:n.928G>A
NM_001080476.2:c.*55G>A NP_001073945.1:n.*55G>A
XM_011513691.1:c.*55G>A XP_011511993.1:n.*55G>A
NM_001080476.3:c.*55G>A MANE Select NP_001073945.1:n.*55G>A
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