Canonical Allele Identifier: CA443658870
Gene: SLC45A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.33944894C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33944789C>T , CM000667.2:g.33944789C>T GRCh38
NC_000005.9:g.33944894C>T , CM000667.1:g.33944894C>T GRCh37
NC_000005.8:g.33980651C>T NCBI36
NG_011691.2:g.44887G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1452G>A MANE Select ENSP00000296589.4:p.Gln484=
ENST00000296589.8:c.1452G>A ENSP00000296589.4:p.Gln484=
NM_016180.4:c.1452G>A NP_057264.3:p.Gln484=
XM_011514051.1:c.1050G>A XP_011512353.1:p.Gln350=
NM_016180.5:c.1452G>A MANE Select NP_057264.4:p.Gln484=
Search 100 bp 5'
Search 100 bp 3'