Canonical Allele Identifier: CA491015653

Gene: SMAD3

Linked Data

• dbSNP Id: rs1959914440
• gnomAD v4: 15-67066292-G-T
• MyVariant Identifiers: chr15:g.67358630G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67066292G>T , CM000677.2:g.67066292G>T	GRCh38
NC_000015.9:g.67358630G>T , CM000677.1:g.67358630G>T	GRCh37
NC_000015.8:g.65145684G>T	NCBI36
NG_011990.1:g.5436G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559460.6:c.-110+2348G>T	ENSP00000453082.2:n.-110+2348G>T
ENST00000560424.2:c.138G>T	ENSP00000455540.2:p.Gly46=
ENST00000327367.9:c.138G>T MANE Select	ENSP00000332973.4:p.Gly46=
ENST00000327367.8:c.138G>T	ENSP00000332973.4:p.Gly46=
ENST00000559460.5:c.-110+2348G>T	ENSP00000453082.1:n.-110+2348G>T
NM_005902.3:c.138G>T	NP_005893.1:p.Gly46=
XM_011521559.1:c.138G>T	XP_011519861.1:p.Gly46=
XM_011521559.3:c.138G>T	XP_011519861.1:p.Gly46=
NM_005902.4:c.138G>T MANE Select	NP_005893.1:p.Gly46=