Canonical Allele Identifier: CA2616608957
Gene: VSIG2 HGNC NCBI

Linked Data

gnomAD v4: 11-124748032-GCTCAGGACAAATCCATTTCCTGGCATCTACAAGCCACTACTA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124748036_124748077del , CM000673.2:g.124748036_124748077del GRCh38
NC_000011.9:g.124617932_124617973del , CM000673.1:g.124617932_124617973del GRCh37
NC_000011.8:g.124123142_124123183del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326621.10:c.851+316_851+357del MANE Select ENSP00000318684.5:n.851+316_851+357del
ENST00000326621.9:c.851+316_851+357del ENSP00000318684.5:n.851+316_851+357del
NM_014312.3:c.851+316_851+357del NP_055127.2:n.851+316_851+357del
XM_011542727.1:c.1211+316_1211+357del XP_011541029.1:n.1211+316_1211+357del
XM_011542728.1:c.845+316_845+357del XP_011541030.1:n.845+316_845+357del
XR_428973.2:n.1642+316_1642+357del
NM_014312.4:c.851+316_851+357del NP_055127.2:n.851+316_851+357del
NM_014312.5:c.851+316_851+357del MANE Select NP_055127.2:n.851+316_851+357del
Search 100 bp 5'
Search 100 bp 3'