Canonical Allele Identifier: CA2649657832
Gene: F13B HGNC NCBI

Linked Data

gnomAD v4: 1-197039335-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039335T>C , CM000663.2:g.197039335T>C GRCh38
NC_000001.10:g.197008465T>C , CM000663.1:g.197008465T>C GRCh37
NC_000001.9:g.195275088T>C NCBI36
NG_012065.1:g.32933A>G , LRG_550:g.32933A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.*43A>G MANE Select ENSP00000356382.2:n.*43A>G
ENST00000649282.1:c.784A>G ENSP00000497116.1:n.784A>G
ENST00000367412.1:c.*43A>G ENSP00000356382.1:n.*43A>G
NM_001994.2:c.*43A>G , LRG_550t1:c.*43A>G NP_001985.2:n.*43A>G
XM_011509283.2:c.*964A>G XP_011507585.1:n.*964A>G
XM_011509284.2:c.*964A>G XP_011507586.1:n.*964A>G
XM_011509286.2:c.*964A>G XP_011507588.1:n.*964A>G
NM_001994.3:c.*43A>G MANE Select NP_001985.2:n.*43A>G
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