Canonical Allele Identifier: CA422667770

Gene: F13B

Linked Data

• MyVariant Identifiers: chr1:g.197024858T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197055728T>G , CM000663.2:g.197055728T>G	GRCh38
NC_000001.10:g.197024858T>G , CM000663.1:g.197024858T>G	GRCh37
NC_000001.9:g.195291481T>G	NCBI36
NG_012065.1:g.16540A>C , LRG_550:g.16540A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1341A>C MANE Select	ENSP00000356382.2:p.Pro447=
ENST00000649282.1:c.96A>C	ENSP00000497116.1:p.Pro32=
ENST00000367412.1:c.1341A>C	ENSP00000356382.1:p.Pro447=
NM_001994.2:c.1341A>C , LRG_550t1:c.1341A>C	NP_001985.2:p.Pro447=
XM_011509283.1:c.1341A>C	XP_011507585.1:p.Pro447=
XM_011509284.1:c.1338A>C	XP_011507586.1:p.Pro446=
XM_011509285.1:c.1245A>C	XP_011507587.1:p.Pro415=
XM_011509286.1:c.1197A>C	XP_011507588.1:p.Pro399=
XM_011509283.2:c.1341A>C	XP_011507585.1:p.Pro447=
XM_011509284.2:c.1338A>C	XP_011507586.1:p.Pro446=
XM_011509286.2:c.1197A>C	XP_011507588.1:p.Pro399=
NM_001994.3:c.1341A>C MANE Select	NP_001985.2:p.Pro447=