Canonical Allele Identifier: CA2670496551
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42963253-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963253T>G , CM000666.2:g.42963253T>G GRCh38
NC_000004.11:g.42965270T>G , CM000666.1:g.42965270T>G GRCh37
NC_000004.10:g.42660027T>G NCBI36
NG_027718.1:g.74988T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+119T>G MANE Select ENSP00000382670.2:n.627+119T>G
ENST00000399770.2:c.627+119T>G ENSP00000382670.2:n.627+119T>G
NM_001080476.2:c.627+119T>G NP_001073945.1:n.627+119T>G
XM_011513691.1:c.264+119T>G XP_011511993.1:n.264+119T>G
NM_001080476.3:c.627+119T>G MANE Select NP_001073945.1:n.627+119T>G
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