Canonical Allele Identifier: CA286899967

Gene: SRR

Linked Data

• dbSNP Id: rs964678696
• gnomAD v3: 17-2312917-A-G
• gnomAD v4: 17-2312917-A-G
• MyVariant Identifiers: chr17:g.2216211A>G (hg19) ; chr17:g.2312917A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2312917A>G , CM000679.2:g.2312917A>G	GRCh38
NC_000017.10:g.2216211A>G , CM000679.1:g.2216211A>G	GRCh37
NC_000017.9:g.2162961A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000344595.10:c.-4-2640A>G MANE Select	ENSP00000339435.5:n.-4-2640A>G
ENST00000344595.9:c.-4-2640A>G	ENSP00000339435.5:n.-4-2640A>G
ENST00000570662.2:c.-4-2640A>G	ENSP00000460581.2:n.-4-2640A>G
ENST00000572709.5:c.-4-2640A>G	ENSP00000458814.1:n.-4-2640A>G
ENST00000574987.1:c.-279-4953A>G	ENSP00000461343.1:n.-279-4953A>G
ENST00000575840.5:c.-4-2640A>G	ENSP00000461589.1:n.-4-2640A>G
ENST00000576620.5:c.-4-2640A>G	ENSP00000461125.1:n.-4-2640A>G
ENST00000576848.1:c.-85+8900A>G	ENSP00000476682.1:n.-85+8900A>G
NM_001304803.1:c.-279-4953A>G	NP_001291732.1:n.-279-4953A>G
NM_021947.2:c.-4-2640A>G	NP_068766.1:n.-4-2640A>G
XM_006721565.2:c.-4-2640A>G	XP_006721628.1:n.-4-2640A>G
XM_006721566.2:c.-4-2640A>G	XP_006721629.1:n.-4-2640A>G
XM_011523974.1:c.-4-2640A>G	XP_011522276.1:n.-4-2640A>G
XM_011523975.1:c.-4-2640A>G	XP_011522277.1:n.-4-2640A>G
XM_006721565.3:c.-4-2640A>G	XP_006721628.1:n.-4-2640A>G
XM_006721566.3:c.-4-2640A>G	XP_006721629.1:n.-4-2640A>G
XM_011523974.3:c.-4-2640A>G	XP_011522276.1:n.-4-2640A>G
NM_021947.3:c.-4-2640A>G MANE Select	NP_068766.1:n.-4-2640A>G