Canonical Allele Identifier: CA1453073692
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748154275
gnomAD v4: 4-42962815-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962820del , CM000666.2:g.42962820del GRCh38
NC_000004.11:g.42964837del , CM000666.1:g.42964837del GRCh37
NC_000004.10:g.42659594del NCBI36
NG_027718.1:g.74555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-72del MANE Select ENSP00000382670.2:n.385-72del
ENST00000399770.2:c.385-72del ENSP00000382670.2:n.385-72del
NM_001080476.2:c.385-72del NP_001073945.1:n.385-72del
XM_011513691.1:c.22-72del XP_011511993.1:n.22-72del
NM_001080476.3:c.385-72del MANE Select NP_001073945.1:n.385-72del
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