Canonical Allele Identifier: CA422667763

Gene: F13B

Linked Data

• MyVariant Identifiers: chr1:g.197024855A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197055725A>C , CM000663.2:g.197055725A>C	GRCh38
NC_000001.10:g.197024855A>C , CM000663.1:g.197024855A>C	GRCh37
NC_000001.9:g.195291478A>C	NCBI36
NG_012065.1:g.16543T>G , LRG_550:g.16543T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1344T>G MANE Select	ENSP00000356382.2:p.Pro448=
ENST00000649282.1:c.99T>G	ENSP00000497116.1:p.Pro33=
ENST00000367412.1:c.1344T>G	ENSP00000356382.1:p.Pro448=
NM_001994.2:c.1344T>G , LRG_550t1:c.1344T>G	NP_001985.2:p.Pro448=
XM_011509283.1:c.1344T>G	XP_011507585.1:p.Pro448=
XM_011509284.1:c.1341T>G	XP_011507586.1:p.Pro447=
XM_011509285.1:c.1248T>G	XP_011507587.1:p.Pro416=
XM_011509286.1:c.1200T>G	XP_011507588.1:p.Pro400=
XM_011509283.2:c.1344T>G	XP_011507585.1:p.Pro448=
XM_011509284.2:c.1341T>G	XP_011507586.1:p.Pro447=
XM_011509286.2:c.1200T>G	XP_011507588.1:p.Pro400=
NM_001994.3:c.1344T>G MANE Select	NP_001985.2:p.Pro448=