Canonical Allele Identifier: CA2649657795

Gene: F13B

Linked Data

• gnomAD v4: 1-197039276-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039276C>A , CM000663.2:g.197039276C>A	GRCh38
NC_000001.10:g.197008406C>A , CM000663.1:g.197008406C>A	GRCh37
NC_000001.9:g.195275029C>A	NCBI36
NG_012065.1:g.32992G>T , LRG_550:g.32992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*102G>T MANE Select	ENSP00000356382.2:n.*102G>T
ENST00000649282.1:c.843G>T	ENSP00000497116.1:n.843G>T
ENST00000367412.1:c.*102G>T	ENSP00000356382.1:n.*102G>T
NM_001994.2:c.*102G>T , LRG_550t1:c.*102G>T	NP_001985.2:n.*102G>T
XM_011509283.2:c.*1023G>T	XP_011507585.1:n.*1023G>T
XM_011509284.2:c.*1023G>T	XP_011507586.1:n.*1023G>T
XM_011509286.2:c.*1023G>T	XP_011507588.1:n.*1023G>T
NM_001994.3:c.*102G>T MANE Select	NP_001985.2:n.*102G>T