Canonical Allele Identifier: CA729740669

Gene: F13B

Linked Data

• dbSNP Id: rs1475068080
• MyVariant Identifiers: chr1:g.197008424T>C (hg19) ; chr1:g.197039294T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039294T>C , CM000663.2:g.197039294T>C	GRCh38
NC_000001.10:g.197008424T>C , CM000663.1:g.197008424T>C	GRCh37
NC_000001.9:g.195275047T>C	NCBI36
NG_012065.1:g.32974A>G , LRG_550:g.32974A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*84A>G MANE Select	ENSP00000356382.2:n.*84A>G
ENST00000649282.1:c.825A>G	ENSP00000497116.1:n.825A>G
ENST00000367412.1:c.*84A>G	ENSP00000356382.1:n.*84A>G
NM_001994.2:c.*84A>G , LRG_550t1:c.*84A>G	NP_001985.2:n.*84A>G
XM_011509283.2:c.*1005A>G	XP_011507585.1:n.*1005A>G
XM_011509284.2:c.*1005A>G	XP_011507586.1:n.*1005A>G
XM_011509286.2:c.*1005A>G	XP_011507588.1:n.*1005A>G
NM_001994.3:c.*84A>G MANE Select	NP_001985.2:n.*84A>G