Canonical Allele Identifier: CA1538206742
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33944790T= , CM000667.2:g.33944790T= GRCh38
NC_000005.9:g.33944895T= , CM000667.1:g.33944895T= GRCh37
NC_000005.8:g.33980652T= NCBI36
NG_011691.2:g.44886A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1451A= MANE Select ENSP00000296589.4:p.Gln484=
ENST00000296589.8:c.1451A= ENSP00000296589.4:p.Gln484=
NM_016180.4:c.1451A= NP_057264.3:p.Gln484=
XM_011514051.1:c.1049A= XP_011512353.1:p.Gln350=
NM_016180.5:c.1451A= MANE Select NP_057264.4:p.Gln484=