Canonical Allele Identifier: CA491071737

Gene: SMAD3

Linked Data

• dbSNP Id: rs1962552595
• gnomAD v4: 15-67165329-C-T
• MyVariant Identifiers: chr15:g.67457667C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67165329C>T , CM000677.2:g.67165329C>T	GRCh38
NC_000015.9:g.67457667C>T , CM000677.1:g.67457667C>T	GRCh37
NC_000015.8:g.65244721C>T	NCBI36
NG_011990.1:g.104473C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.162C>T	ENSP00000453684.2:p.Ser54=
ENST00000559460.6:c.162C>T	ENSP00000453082.2:p.Ser54=
ENST00000560424.2:c.477C>T	ENSP00000455540.2:p.Ser159=
ENST00000327367.9:c.477C>T MANE Select	ENSP00000332973.4:p.Ser159=
ENST00000679624.1:c.162C>T	ENSP00000505445.1:p.Ser54=
ENST00000681239.1:c.162C>T	ENSP00000505641.1:p.Ser54=
ENST00000327367.8:c.477C>T	ENSP00000332973.4:p.Ser159=
ENST00000439724.7:c.345C>T	ENSP00000401133.3:p.Ser115=
ENST00000540846.6:c.162C>T	ENSP00000437757.2:p.Ser54=
ENST00000558739.1:c.162C>T	ENSP00000453684.1:p.Ser54=
ENST00000558894.5:c.162C>T	ENSP00000458060.1:p.Ser54=
ENST00000559460.5:c.162C>T	ENSP00000453082.1:p.Ser54=
ENST00000559937.1:n.327C>T
ENST00000560175.5:c.162C>T	ENSP00000455095.1:p.Ser54=
NM_001145102.1:c.162C>T	NP_001138574.1:p.Ser54=
NM_001145103.1:c.345C>T	NP_001138575.1:p.Ser115=
NM_005902.3:c.477C>T	NP_005893.1:p.Ser159=
XM_011521559.1:c.400+241C>T	XP_011519861.1:n.400+241C>T
XM_011521560.1:c.330C>T	XP_011519862.1:p.Ser110=
XM_011521559.3:c.400+241C>T	XP_011519861.1:n.400+241C>T
NM_005902.4:c.477C>T MANE Select	NP_005893.1:p.Ser159=
NM_001145102.2:c.162C>T	NP_001138574.1:p.Ser54=
NM_001145103.2:c.345C>T	NP_001138575.1:p.Ser115=