Canonical Allele Identifier: CA256475888

Gene: F10

Linked Data

• dbSNP Id: rs79156180
• gnomAD v3: 13-113139536-A-G
• gnomAD v4: 13-113139536-A-G
• MyVariant Identifiers: chr13:g.113793850A>G (hg19) ; chr13:g.113139536A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113139536A>G , CM000675.2:g.113139536A>G	GRCh38
NC_000013.10:g.113793850A>G , CM000675.1:g.113793850A>G	GRCh37
NC_000013.9:g.112841851A>G	NCBI36
NG_009258.1:g.21738A>G , LRG_548:g.21738A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.370+66A>G MANE Select	ENSP00000364709.3:n.370+66A>G
ENST00000375551.7:c.370+66A>G	ENSP00000364701.3:n.370+66A>G
ENST00000375559.7:c.370+66A>G	ENSP00000364709.3:n.370+66A>G
ENST00000409306.5:c.370+66A>G	ENSP00000387092.1:n.370+66A>G
ENST00000410083.6:c.370+66A>G	ENSP00000386320.2:n.370+66A>G
ENST00000477269.5:n.407+66A>G
NM_000504.3:c.370+66A>G , LRG_548t1:c.370+66A>G	NP_000495.1:n.370+66A>G
NM_001312674.1:c.370+66A>G	NP_001299603.1:n.370+66A>G
NM_001312675.1:c.370+66A>G	NP_001299604.1:n.370+66A>G
NM_000504.4:c.370+66A>G MANE Select	NP_000495.1:n.370+66A>G
NM_001312674.2:c.370+66A>G	NP_001299603.1:n.370+66A>G
NM_001312675.2:c.370+66A>G	NP_001299604.1:n.370+66A>G