Canonical Allele Identifier: CA35869291

Gene: F13B

Linked Data

• dbSNP Id: rs545688760
• MyVariant Identifiers: chr1:g.197008325A>C (hg19) ; chr1:g.197039195A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039195A>C , CM000663.2:g.197039195A>C	GRCh38
NC_000001.10:g.197008325A>C , CM000663.1:g.197008325A>C	GRCh37
NC_000001.9:g.195274948A>C	NCBI36
NG_012065.1:g.33073T>G , LRG_550:g.33073T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*183T>G MANE Select	ENSP00000356382.2:n.*183T>G
ENST00000649282.1:c.924T>G	ENSP00000497116.1:n.924T>G
ENST00000367412.1:c.*183T>G	ENSP00000356382.1:n.*183T>G
NM_001994.2:c.*183T>G , LRG_550t1:c.*183T>G	NP_001985.2:n.*183T>G
XM_011509283.2:c.*1104T>G	XP_011507585.1:n.*1104T>G
XM_011509284.2:c.*1104T>G	XP_011507586.1:n.*1104T>G
XM_011509286.2:c.*1104T>G	XP_011507588.1:n.*1104T>G
NM_001994.3:c.*183T>G MANE Select	NP_001985.2:n.*183T>G