Canonical Allele Identifier: CA2649657825
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039329-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039329G>C , CM000663.2:g.197039329G>C GRCh38
NC_000001.10:g.197008459G>C , CM000663.1:g.197008459G>C GRCh37
NC_000001.9:g.195275082G>C NCBI36
NG_012065.1:g.32939C>G , LRG_550:g.32939C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.*49C>G MANE Select ENSP00000356382.2:n.*49C>G
ENST00000649282.1:c.790C>G ENSP00000497116.1:n.790C>G
ENST00000367412.1:c.*49C>G ENSP00000356382.1:n.*49C>G
NM_001994.2:c.*49C>G , LRG_550t1:c.*49C>G NP_001985.2:n.*49C>G
XM_011509283.2:c.*970C>G XP_011507585.1:n.*970C>G
XM_011509284.2:c.*970C>G XP_011507586.1:n.*970C>G
XM_011509286.2:c.*970C>G XP_011507588.1:n.*970C>G
NM_001994.3:c.*49C>G MANE Select NP_001985.2:n.*49C>G
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