Canonical Allele Identifier: CA344000923
Gene: F13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197055730G>C , CM000663.2:g.197055730G>C GRCh38
NC_000001.10:g.197024860G>C , CM000663.1:g.197024860G>C GRCh37
NC_000001.9:g.195291483G>C NCBI36
NG_012065.1:g.16538C>G , LRG_550:g.16538C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.1339C>G MANE Select ENSP00000356382.2:p.Pro447Ala
ENST00000649282.1:c.94C>G ENSP00000497116.1:p.Pro32Ala
ENST00000367412.1:c.1339C>G ENSP00000356382.1:p.Pro447Ala
NM_001994.2:c.1339C>G , LRG_550t1:c.1339C>G NP_001985.2:p.Pro447Ala
XM_011509283.1:c.1339C>G XP_011507585.1:p.Pro447Ala
XM_011509284.1:c.1336C>G XP_011507586.1:p.Pro446Ala
XM_011509285.1:c.1243C>G XP_011507587.1:p.Pro415Ala
XM_011509286.1:c.1195C>G XP_011507588.1:p.Pro399Ala
XM_011509283.2:c.1339C>G XP_011507585.1:p.Pro447Ala
XM_011509284.2:c.1336C>G XP_011507586.1:p.Pro446Ala
XM_011509286.2:c.1195C>G XP_011507588.1:p.Pro399Ala
NM_001994.3:c.1339C>G MANE Select NP_001985.2:p.Pro447Ala