Canonical Allele Identifier: CA7764579

Gene: TM2D3

Linked Data

• dbSNP Id: rs757550832
• ExAC: 15:102186917 C / T
• gnomAD v3: 15-101646714-C-T
• gnomAD v4: 15-101646714-C-T
• MyVariant Identifiers: chr15:g.102186917C>T (hg19) ; chr15:g.101646714C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101646714C>T , CM000677.2:g.101646714C>T	GRCh38
NC_000015.9:g.102186917C>T , CM000677.1:g.102186917C>T	GRCh37
NC_000015.8:g.100004440C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333202.8:c.502+11G>A MANE Select	ENSP00000330433.3:n.502+11G>A
ENST00000333202.7:c.502+11G>A	ENSP00000330433.3:n.502+11G>A
ENST00000347970.7:c.424+11G>A	ENSP00000327584.3:n.424+11G>A
ENST00000428002.6:c.424+11G>A	ENSP00000402179.2:n.424+11G>A
ENST00000558129.5:c.333+11G>A
ENST00000558677.5:c.803+11G>A
ENST00000559024.5:n.534G>A
ENST00000559107.5:c.502+11G>A	ENSP00000454131.1:n.502+11G>A
ENST00000560013.5:c.*870+11G>A	ENSP00000453503.1:n.*870+11G>A
ENST00000560910.5:n.455G>A
ENST00000561373.1:c.307+11G>A	ENSP00000452823.1:n.307+11G>A
NM_001307960.1:c.424+11G>A	NP_001294889.1:n.424+11G>A
NM_001308026.1:c.502+11G>A	NP_001294955.1:n.502+11G>A
NM_025141.3:c.424+11G>A	NP_079417.2:n.424+11G>A
NM_078474.2:c.502+11G>A	NP_510883.2:n.502+11G>A
NM_078474.3:c.502+11G>A MANE Select	NP_510883.2:n.502+11G>A
NM_001307960.2:c.424+11G>A	NP_001294889.1:n.424+11G>A
NM_001308026.2:c.502+11G>A	NP_001294955.1:n.502+11G>A
NM_025141.4:c.424+11G>A	NP_079417.2:n.424+11G>A