Canonical Allele Identifier: CA1955682492
Gene: SPTY2D1 HGNC NCBI

Linked Data

dbSNP Id: rs1590399221

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611439G>A , CM000673.2:g.18611439G>A GRCh38
NC_000011.9:g.18632986G>A , CM000673.1:g.18632986G>A GRCh37
NC_000011.8:g.18589562G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+38C>T MANE Select ENSP00000337991.5:n.1964+38C>T
ENST00000336349.5:c.1964+38C>T ENSP00000337991.5:n.1964+38C>T
NM_194285.2:c.1964+38C>T NP_919261.2:n.1964+38C>T
XM_011519919.1:c.1712+38C>T XP_011518221.1:n.1712+38C>T
XM_011519919.2:c.1712+38C>T XP_011518221.1:n.1712+38C>T
NM_194285.3:c.1964+38C>T MANE Select NP_919261.2:n.1964+38C>T