Canonical Allele Identifier: CA5913058
Gene: SPTY2D1 HGNC NCBI

Linked Data

dbSNP Id: rs748300471

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611467T>G , CM000673.2:g.18611467T>G GRCh38
NC_000011.9:g.18633014T>G , CM000673.1:g.18633014T>G GRCh37
NC_000011.8:g.18589590T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+10A>C MANE Select ENSP00000337991.5:n.1964+10A>C
ENST00000336349.5:c.1964+10A>C ENSP00000337991.5:n.1964+10A>C
NM_194285.2:c.1964+10A>C NP_919261.2:n.1964+10A>C
XM_011519919.1:c.1712+10A>C XP_011518221.1:n.1712+10A>C
XM_011519919.2:c.1712+10A>C XP_011518221.1:n.1712+10A>C
NM_194285.3:c.1964+10A>C MANE Select NP_919261.2:n.1964+10A>C