Canonical Allele Identifier: CA1522520690

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213851C= , CM000667.2:g.1213851C=	GRCh38
NC_000005.9:g.1213966C= , CM000667.1:g.1213966C=	GRCh37
NC_000005.8:g.1266966C=	NCBI36
NG_008282.1:g.17257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.775-102C= MANE Select	ENSP00000305302.10:n.775-102C=
ENST00000304460.10:c.775-102C=	ENSP00000305302.10:n.775-102C=
ENST00000515652.5:c.683-102C=	ENSP00000425701.1:n.683-102C=
NM_001003841.2:c.775-102C=	NP_001003841.1:n.775-102C=
NM_001003841.3:c.775-102C= MANE Select	NP_001003841.1:n.775-102C=