Canonical Allele Identifier: CA2616608999
Gene: VSIG2 HGNC NCBI

Linked Data

gnomAD v4: 11-124748056-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124748056C>A , CM000673.2:g.124748056C>A GRCh38
NC_000011.9:g.124617952C>A , CM000673.1:g.124617952C>A GRCh37
NC_000011.8:g.124123162C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326621.10:c.851+334G>T MANE Select ENSP00000318684.5:n.851+334G>T
ENST00000326621.9:c.851+334G>T ENSP00000318684.5:n.851+334G>T
NM_014312.3:c.851+334G>T NP_055127.2:n.851+334G>T
XM_011542727.1:c.1211+334G>T XP_011541029.1:n.1211+334G>T
XM_011542728.1:c.845+334G>T XP_011541030.1:n.845+334G>T
XR_428973.2:n.1642+334G>T
NM_014312.4:c.851+334G>T NP_055127.2:n.851+334G>T
NM_014312.5:c.851+334G>T MANE Select NP_055127.2:n.851+334G>T
Search 100 bp 5'
Search 100 bp 3'