Canonical Allele Identifier: CA439191612
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42963017-T-C
MyVariant Identifiers: chr4:g.42965034T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963017T>C , CM000666.2:g.42963017T>C GRCh38
NC_000004.11:g.42965034T>C , CM000666.1:g.42965034T>C GRCh37
NC_000004.10:g.42659791T>C NCBI36
NG_027718.1:g.74752T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.510T>C MANE Select ENSP00000382670.2:p.Phe170=
ENST00000399770.2:c.510T>C ENSP00000382670.2:p.Phe170=
NM_001080476.2:c.510T>C NP_001073945.1:p.Phe170=
XM_011513691.1:c.147T>C XP_011511993.1:p.Phe49=
NM_001080476.3:c.510T>C MANE Select NP_001073945.1:p.Phe170=
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