Canonical Allele Identifier: CA1206117317
Gene: SLC19A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485592C= , CM000663.2:g.169485592C= GRCh38
NC_000001.10:g.169454830C= , CM000663.1:g.169454830C= GRCh37
NC_000001.9:g.167721454C= NCBI36
NG_008255.1:g.5379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000236137.10:c.175G= MANE Select ENSP00000236137.5:p.Gly59=
ENST00000646596.1:c.175G= ENSP00000494404.1:p.Gly59=
ENST00000236137.9:c.175G= ENSP00000236137.5:p.Gly59=
ENST00000367804.4:c.175G= ENSP00000356778.3:p.Gly59=
NM_006996.2:c.175G= NP_008927.1:p.Gly59=
XM_011509076.1:c.12+461G= XP_011507378.1:n.12+461G=
XM_011509077.1:c.175G= XP_011507379.1:p.Gly59=
NM_001319667.1:c.175G= NP_001306596.1:p.Gly59=
NM_006996.3:c.175G= MANE Select NP_008927.1:p.Gly59=