Canonical Allele Identifier: CA1453073875
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963171C= , CM000666.2:g.42963171C= GRCh38
NC_000004.11:g.42965188C= , CM000666.1:g.42965188C= GRCh37
NC_000004.10:g.42659945C= NCBI36
NG_027718.1:g.74906C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+37C= MANE Select ENSP00000382670.2:n.627+37C=
ENST00000399770.2:c.627+37C= ENSP00000382670.2:n.627+37C=
NM_001080476.2:c.627+37C= NP_001073945.1:n.627+37C=
XM_011513691.1:c.264+37C= XP_011511993.1:n.264+37C=
NM_001080476.3:c.627+37C= MANE Select NP_001073945.1:n.627+37C=
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