Canonical Allele Identifier: CA356792091
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs865779528
gnomAD v4: 4-42962891-G-C
MyVariant Identifiers: chr4:g.42964908G>C (hg19) chr4:g.42962891G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962891G>C , CM000666.2:g.42962891G>C GRCh38
NC_000004.11:g.42964908G>C , CM000666.1:g.42964908G>C GRCh37
NC_000004.10:g.42659665G>C NCBI36
NG_027718.1:g.74626G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-1G>C MANE Select ENSP00000382670.2:n.385-1G>C
ENST00000399770.2:c.385-1G>C ENSP00000382670.2:n.385-1G>C
NM_001080476.2:c.385-1G>C NP_001073945.1:n.385-1G>C
XM_011513691.1:c.22-1G>C XP_011511993.1:n.22-1G>C
NM_001080476.3:c.385-1G>C MANE Select NP_001073945.1:n.385-1G>C
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