Canonical Allele Identifier: CA674317371
Gene: SPTY2D1 HGNC NCBI

Linked Data

dbSNP Id: rs1445227982

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611444T>C , CM000673.2:g.18611444T>C GRCh38
NC_000011.9:g.18632991T>C , CM000673.1:g.18632991T>C GRCh37
NC_000011.8:g.18589567T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+33A>G MANE Select ENSP00000337991.5:n.1964+33A>G
ENST00000336349.5:c.1964+33A>G ENSP00000337991.5:n.1964+33A>G
NM_194285.2:c.1964+33A>G NP_919261.2:n.1964+33A>G
XM_011519919.1:c.1712+33A>G XP_011518221.1:n.1712+33A>G
XM_011519919.2:c.1712+33A>G XP_011518221.1:n.1712+33A>G
NM_194285.3:c.1964+33A>G MANE Select NP_919261.2:n.1964+33A>G