Canonical Allele Identifier: CA35869280
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs556119836
gnomAD v2: 1-197008300-T-C
gnomAD v3: 1-197039170-T-C
gnomAD v4: 1-197039170-T-C
MyVariant Identifiers: chr1:g.197008300T>C (hg19) chr1:g.197039170T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039170T>C , CM000663.2:g.197039170T>C GRCh38
NC_000001.10:g.197008300T>C , CM000663.1:g.197008300T>C GRCh37
NC_000001.9:g.195274923T>C NCBI36
NG_012065.1:g.33098A>G , LRG_550:g.33098A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*208A>G MANE Select ENSP00000356382.2:n.*208A>G
ENST00000649282.1:c.949A>G ENSP00000497116.1:n.949A>G
XM_011509283.2:c.*1129A>G XP_011507585.1:n.*1129A>G
XM_011509284.2:c.*1129A>G XP_011507586.1:n.*1129A>G
XM_011509286.2:c.*1129A>G XP_011507588.1:n.*1129A>G
NM_001994.3:c.*208A>G MANE Select NP_001985.2:n.*208A>G
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