Canonical Allele Identifier: CA2649657708

Gene: F13B

Linked Data

• gnomAD v4: 1-197039203-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039203T>C , CM000663.2:g.197039203T>C	GRCh38
NC_000001.10:g.197008333T>C , CM000663.1:g.197008333T>C	GRCh37
NC_000001.9:g.195274956T>C	NCBI36
NG_012065.1:g.33065A>G , LRG_550:g.33065A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*175A>G MANE Select	ENSP00000356382.2:n.*175A>G
ENST00000649282.1:c.916A>G	ENSP00000497116.1:n.916A>G
ENST00000367412.1:c.*175A>G	ENSP00000356382.1:n.*175A>G
NM_001994.2:c.*175A>G , LRG_550t1:c.*175A>G	NP_001985.2:n.*175A>G
XM_011509283.2:c.*1096A>G	XP_011507585.1:n.*1096A>G
XM_011509284.2:c.*1096A>G	XP_011507586.1:n.*1096A>G
XM_011509286.2:c.*1096A>G	XP_011507588.1:n.*1096A>G
NM_001994.3:c.*175A>G MANE Select	NP_001985.2:n.*175A>G