Canonical Allele Identifier: CA2649031398

Gene: SLC19A2

Linked Data

• gnomAD v4: 1-169485427-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485427A>G , CM000663.2:g.169485427A>G	GRCh38
NC_000001.10:g.169454665A>G , CM000663.1:g.169454665A>G	GRCh37
NC_000001.9:g.167721289A>G	NCBI36
NG_008255.1:g.5544T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+136T>C MANE Select	ENSP00000236137.5:n.204+136T>C
ENST00000646596.1:c.204+136T>C	ENSP00000494404.1:n.204+136T>C
ENST00000236137.9:c.204+136T>C	ENSP00000236137.5:n.204+136T>C
ENST00000367804.4:c.204+136T>C	ENSP00000356778.3:n.204+136T>C
NM_006996.2:c.204+136T>C	NP_008927.1:n.204+136T>C
XM_011509076.1:c.12+626T>C	XP_011507378.1:n.12+626T>C
XM_011509077.1:c.204+136T>C	XP_011507379.1:n.204+136T>C
NM_001319667.1:c.204+136T>C	NP_001306596.1:n.204+136T>C
NM_006996.3:c.204+136T>C MANE Select	NP_008927.1:n.204+136T>C