Canonical Allele Identifier: CA343112122
Gene: SLC19A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485589G>C , CM000663.2:g.169485589G>C GRCh38
NC_000001.10:g.169454827G>C , CM000663.1:g.169454827G>C GRCh37
NC_000001.9:g.167721451G>C NCBI36
NG_008255.1:g.5382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000236137.10:c.178C>G MANE Select ENSP00000236137.5:p.Pro60Ala
ENST00000646596.1:c.178C>G ENSP00000494404.1:p.Pro60Ala
ENST00000236137.9:c.178C>G ENSP00000236137.5:p.Pro60Ala
ENST00000367804.4:c.178C>G ENSP00000356778.3:p.Pro60Ala
NM_006996.2:c.178C>G NP_008927.1:p.Pro60Ala
XM_011509076.1:c.12+464C>G XP_011507378.1:n.12+464C>G
XM_011509077.1:c.178C>G XP_011507379.1:p.Pro60Ala
NM_001319667.1:c.178C>G NP_001306596.1:p.Pro60Ala
NM_006996.3:c.178C>G MANE Select NP_008927.1:p.Pro60Ala