Canonical Allele Identifier: CA1217904189
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs1654950549
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039304A>G , CM000663.2:g.197039304A>G GRCh38
NC_000001.10:g.197008434A>G , CM000663.1:g.197008434A>G GRCh37
NC_000001.9:g.195275057A>G NCBI36
NG_012065.1:g.32964T>C , LRG_550:g.32964T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.*74T>C MANE Select ENSP00000356382.2:n.*74T>C
ENST00000649282.1:c.815T>C ENSP00000497116.1:n.815T>C
ENST00000367412.1:c.*74T>C ENSP00000356382.1:n.*74T>C
NM_001994.2:c.*74T>C , LRG_550t1:c.*74T>C NP_001985.2:n.*74T>C
XM_011509283.2:c.*995T>C XP_011507585.1:n.*995T>C
XM_011509284.2:c.*995T>C XP_011507586.1:n.*995T>C
XM_011509286.2:c.*995T>C XP_011507588.1:n.*995T>C
NM_001994.3:c.*74T>C MANE Select NP_001985.2:n.*74T>C
Search 100 bp 5'
Search 100 bp 3'