Canonical Allele Identifier: CA619152941

Gene: SIN3A

Linked Data

• dbSNP Id: rs8028182
• gnomAD v2: 15-75718669-G-C
• gnomAD v3: 15-75426328-G-C
• gnomAD v4: 15-75426328-G-C
• MyVariant Identifiers: chr15:g.75718669G>C (hg19) ; chr15:g.75426328G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75426328G>C , CM000677.2:g.75426328G>C	GRCh38
NC_000015.9:g.75718669G>C , CM000677.1:g.75718669G>C	GRCh37
NC_000015.8:g.73505722G>C	NCBI36
NG_052855.1:g.34456C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000564778.6:c.190-3505C>G	ENSP00000455204.2:n.190-3505C>G
ENST00000565264.2:c.190-3505C>G	ENSP00000454296.2:n.190-3505C>G
ENST00000704304.1:c.190-3054C>G	ENSP00000515828.1:n.190-3054C>G
ENST00000704305.1:c.190-3054C>G	ENSP00000515829.1:n.190-3054C>G
ENST00000704310.1:c.190-3505C>G	ENSP00000515832.1:n.190-3505C>G
ENST00000704312.1:c.190-3505C>G	ENSP00000515834.1:n.190-3505C>G
ENST00000394947.8:c.190-3505C>G MANE Select	ENSP00000378402.3:n.190-3505C>G
ENST00000360439.8:c.190-3505C>G	ENSP00000353622.4:n.190-3505C>G
ENST00000394947.7:c.190-3505C>G	ENSP00000378402.3:n.190-3505C>G
ENST00000394949.8:c.190-3505C>G	ENSP00000378403.4:n.190-3505C>G
ENST00000562776.5:c.190-3505C>G	ENSP00000455072.1:n.190-3505C>G
ENST00000564778.5:c.190-3505C>G	ENSP00000455204.1:n.190-3505C>G
ENST00000567289.5:c.190-3505C>G	ENSP00000455834.1:n.190-3505C>G
ENST00000568190.1:c.190-3505C>G	ENSP00000456997.1:n.190-3505C>G
ENST00000568309.5:c.190-3505C>G	ENSP00000455644.1:n.190-3505C>G
ENST00000568431.5:c.190-3505C>G	ENSP00000454750.1:n.190-3505C>G
ENST00000570115.5:c.190-3505C>G	ENSP00000455662.1:n.190-3505C>G
NM_001145357.1:c.190-3505C>G	NP_001138829.1:n.190-3505C>G
NM_001145358.1:c.190-3505C>G	NP_001138830.1:n.190-3505C>G
NM_015477.2:c.190-3505C>G	NP_056292.1:n.190-3505C>G
XM_006720465.2:c.190-3505C>G	XP_006720528.1:n.190-3505C>G
XM_006720466.2:c.190-3505C>G	XP_006720529.1:n.190-3505C>G
XM_006720467.2:c.190-3505C>G	XP_006720530.1:n.190-3505C>G
XM_006720465.3:c.190-3505C>G	XP_006720528.1:n.190-3505C>G
XM_006720466.3:c.190-3505C>G	XP_006720529.1:n.190-3505C>G
XM_006720467.3:c.190-3505C>G	XP_006720530.1:n.190-3505C>G
XM_024449896.1:c.190-3505C>G	XP_024305664.1:n.190-3505C>G
NM_001145357.2:c.190-3505C>G	NP_001138829.1:n.190-3505C>G
NM_001145358.2:c.190-3505C>G MANE Select	NP_001138830.1:n.190-3505C>G
NM_015477.3:c.190-3505C>G	NP_056292.1:n.190-3505C>G