Canonical Allele Identifier: CA96311698
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs199749797
gnomAD v3: 4-42963240-G-GT
gnomAD v4: 4-42963240-G-GT
MyVariant Identifiers: chr4:g.42965257_42965258insT (hg19) chr4:g.42963240_42963241insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963247dup , CM000666.2:g.42963247dup GRCh38
NC_000004.11:g.42965264dup , CM000666.1:g.42965264dup GRCh37
NC_000004.10:g.42660021dup NCBI36
NG_027718.1:g.74982dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+113dup MANE Select ENSP00000382670.2:n.627+113dup
ENST00000399770.2:c.627+113dup ENSP00000382670.2:n.627+113dup
NM_001080476.2:c.627+113dup NP_001073945.1:n.627+113dup
XM_011513691.1:c.264+113dup XP_011511993.1:n.264+113dup
NM_001080476.3:c.627+113dup MANE Select NP_001073945.1:n.627+113dup
Search 100 bp 5'
Search 100 bp 3'