Canonical Allele Identifier: CA96311699
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs199749797
gnomAD v2: 4-42965257-GT-G
gnomAD v3: 4-42963240-GT-G
gnomAD v4: 4-42963240-GT-G
MyVariant Identifiers: chr4:g.42965258del (hg19) chr4:g.42963241del (hg38)
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Genomic Alleles

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

Transcript Alleles

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