Canonical Allele Identifier: CA2612763909
Gene: SPTY2D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611455G>T , CM000673.2:g.18611455G>T GRCh38
NC_000011.9:g.18633002G>T , CM000673.1:g.18633002G>T GRCh37
NC_000011.8:g.18589578G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+22C>A MANE Select ENSP00000337991.5:n.1964+22C>A
ENST00000336349.5:c.1964+22C>A ENSP00000337991.5:n.1964+22C>A
NM_194285.2:c.1964+22C>A NP_919261.2:n.1964+22C>A
XM_011519919.1:c.1712+22C>A XP_011518221.1:n.1712+22C>A
XM_011519919.2:c.1712+22C>A XP_011518221.1:n.1712+22C>A
NM_194285.3:c.1964+22C>A MANE Select NP_919261.2:n.1964+22C>A