Canonical Allele Identifier: CA1453073907
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748168654
gnomAD v4: 4-42963217-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963217C>T , CM000666.2:g.42963217C>T GRCh38
NC_000004.11:g.42965234C>T , CM000666.1:g.42965234C>T GRCh37
NC_000004.10:g.42659991C>T NCBI36
NG_027718.1:g.74952C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+83C>T MANE Select ENSP00000382670.2:n.627+83C>T
ENST00000399770.2:c.627+83C>T ENSP00000382670.2:n.627+83C>T
NM_001080476.2:c.627+83C>T NP_001073945.1:n.627+83C>T
XM_011513691.1:c.264+83C>T XP_011511993.1:n.264+83C>T
NM_001080476.3:c.627+83C>T MANE Select NP_001073945.1:n.627+83C>T
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