Canonical Allele Identifier: CA473389586
Gene: SPTY2D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.18633029T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611482T>C , CM000673.2:g.18611482T>C GRCh38
NC_000011.9:g.18633029T>C , CM000673.1:g.18633029T>C GRCh37
NC_000011.8:g.18589605T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336349.6:c.1959A>G MANE Select ENSP00000337991.5:p.Ala653=
ENST00000336349.5:c.1959A>G ENSP00000337991.5:p.Ala653=
NM_194285.2:c.1959A>G NP_919261.2:p.Ala653=
XM_011519919.1:c.1707A>G XP_011518221.1:p.Ala569=
XM_011519919.2:c.1707A>G XP_011518221.1:p.Ala569=
NM_194285.3:c.1959A>G MANE Select NP_919261.2:p.Ala653=