Canonical Allele Identifier: CA2625651068
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259812-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259812_74259813insA , CM000676.2:g.74259812_74259813insA GRCh38
NC_000014.8:g.74726515_74726516insA , CM000676.1:g.74726515_74726516insA GRCh37
NC_000014.7:g.73796268_73796269insA NCBI36
NG_013092.1:g.25341_25342insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+30_760+31insA MANE Select ENSP00000261980.2:n.760+30_760+31insA
ENST00000261980.2:c.760+30_760+31insA ENSP00000261980.2:n.760+30_760+31insA
NM_182894.2:c.760+30_760+31insA NP_878314.1:n.760+30_760+31insA
XM_011536719.1:c.760+30_760+31insA XP_011535021.1:n.760+30_760+31insA
NM_182894.3:c.760+30_760+31insA MANE Select NP_878314.1:n.760+30_760+31insA
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