Canonical Allele Identifier: CA151207308

Gene: SLC22A3

Linked Data

• dbSNP Id: rs774856869
• gnomAD v2: 6-160863488-G-T
• gnomAD v3: 6-160442456-G-T
• gnomAD v4: 6-160442456-G-T
• MyVariant Identifiers: chr6:g.160863488G>T (hg19) ; chr6:g.160442456G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160442456G>T , CM000668.2:g.160442456G>T	GRCh38
NC_000006.11:g.160863488G>T , CM000668.1:g.160863488G>T	GRCh37
NC_000006.10:g.160783478G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.1289-305G>T MANE Select	ENSP00000275300.2:n.1289-305G>T
ENST00000275300.2:c.1289-305G>T	ENSP00000275300.2:n.1289-305G>T
NM_021977.3:c.1289-305G>T	NP_068812.1:n.1289-305G>T
XM_005267106.3:c.896-305G>T	XP_005267163.1:n.896-305G>T
XM_011536075.1:c.833-305G>T	XP_011534377.1:n.833-305G>T
XM_011536076.1:c.833-305G>T	XP_011534378.1:n.833-305G>T
XM_011536077.1:c.833-305G>T	XP_011534379.1:n.833-305G>T
XR_245546.1:n.1018-305G>T
XM_005267106.5:c.896-305G>T	XP_005267163.1:n.896-305G>T
XM_011536075.2:c.833-305G>T	XP_011534377.1:n.833-305G>T
XM_011536076.3:c.833-305G>T	XP_011534378.1:n.833-305G>T
XM_017011203.2:c.833-305G>T	XP_016866692.1:n.833-305G>T
XR_001743588.1:n.1233-305G>T
XR_001743589.1:n.1018-305G>T
NM_021977.4:c.1289-305G>T MANE Select	NP_068812.1:n.1289-305G>T