Canonical Allele Identifier: CA1061625454
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748171462
gnomAD v3: 4-42963345-CA-C
gnomAD v4: 4-42963345-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963347del , CM000666.2:g.42963347del GRCh38
NC_000004.11:g.42965364del , CM000666.1:g.42965364del GRCh37
NC_000004.10:g.42660121del NCBI36
NG_027718.1:g.75082del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+213del MANE Select ENSP00000382670.2:n.627+213del
ENST00000399770.2:c.627+213del ENSP00000382670.2:n.627+213del
NM_001080476.2:c.627+213del NP_001073945.1:n.627+213del
XM_011513691.1:c.264+213del XP_011511993.1:n.264+213del
NM_001080476.3:c.627+213del MANE Select NP_001073945.1:n.627+213del
Search 100 bp 5'
Search 100 bp 3'