Canonical Allele Identifier: CA356792235
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42962966-T-G
MyVariant Identifiers: chr4:g.42964983T>G (hg19) chr4:g.42962966T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962966T>G , CM000666.2:g.42962966T>G GRCh38
NC_000004.11:g.42964983T>G , CM000666.1:g.42964983T>G GRCh37
NC_000004.10:g.42659740T>G NCBI36
NG_027718.1:g.74701T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.459T>G MANE Select ENSP00000382670.2:p.Phe153Leu
ENST00000399770.2:c.459T>G ENSP00000382670.2:p.Phe153Leu
NM_001080476.2:c.459T>G NP_001073945.1:p.Phe153Leu
XM_011513691.1:c.96T>G XP_011511993.1:p.Phe32Leu
NM_001080476.3:c.459T>G MANE Select NP_001073945.1:p.Phe153Leu
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