Canonical Allele Identifier: CA422667773

Gene: F13B

Linked Data

• gnomAD v4: 1-197055731-G-T
• MyVariant Identifiers: chr1:g.197024861G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197055731G>T , CM000663.2:g.197055731G>T	GRCh38
NC_000001.10:g.197024861G>T , CM000663.1:g.197024861G>T	GRCh37
NC_000001.9:g.195291484G>T	NCBI36
NG_012065.1:g.16537C>A , LRG_550:g.16537C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1338C>A MANE Select	ENSP00000356382.2:p.Ser446=
ENST00000649282.1:c.93C>A	ENSP00000497116.1:p.Ser31=
ENST00000367412.1:c.1338C>A	ENSP00000356382.1:p.Ser446=
NM_001994.2:c.1338C>A , LRG_550t1:c.1338C>A	NP_001985.2:p.Ser446=
XM_011509283.1:c.1338C>A	XP_011507585.1:p.Ser446=
XM_011509284.1:c.1335C>A	XP_011507586.1:p.Ser445=
XM_011509285.1:c.1242C>A	XP_011507587.1:p.Ser414=
XM_011509286.1:c.1194C>A	XP_011507588.1:p.Ser398=
XM_011509283.2:c.1338C>A	XP_011507585.1:p.Ser446=
XM_011509284.2:c.1335C>A	XP_011507586.1:p.Ser445=
XM_011509286.2:c.1194C>A	XP_011507588.1:p.Ser398=
NM_001994.3:c.1338C>A MANE Select	NP_001985.2:p.Ser446=