Canonical Allele Identifier: CA96311680
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs770677946
gnomAD v4: 4-42962902-C-A
MyVariant Identifiers: chr4:g.42964919C>A (hg19) chr4:g.42962902C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962902C>A , CM000666.2:g.42962902C>A GRCh38
NC_000004.11:g.42964919C>A , CM000666.1:g.42964919C>A GRCh37
NC_000004.10:g.42659676C>A NCBI36
NG_027718.1:g.74637C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.395C>A MANE Select ENSP00000382670.2:p.Thr132Asn
ENST00000399770.2:c.395C>A ENSP00000382670.2:p.Thr132Asn
NM_001080476.2:c.395C>A NP_001073945.1:p.Thr132Asn
XM_011513691.1:c.32C>A XP_011511993.1:p.Thr11Asn
NM_001080476.3:c.395C>A MANE Select NP_001073945.1:p.Thr132Asn
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