Canonical Allele Identifier: CA2574775775
Gene: SPTY2D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611458T>C , CM000673.2:g.18611458T>C GRCh38
NC_000011.9:g.18633005T>C , CM000673.1:g.18633005T>C GRCh37
NC_000011.8:g.18589581T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+19A>G MANE Select ENSP00000337991.5:n.1964+19A>G
ENST00000336349.5:c.1964+19A>G ENSP00000337991.5:n.1964+19A>G
NM_194285.2:c.1964+19A>G NP_919261.2:n.1964+19A>G
XM_011519919.1:c.1712+19A>G XP_011518221.1:n.1712+19A>G
XM_011519919.2:c.1712+19A>G XP_011518221.1:n.1712+19A>G
NM_194285.3:c.1964+19A>G MANE Select NP_919261.2:n.1964+19A>G