Canonical Allele Identifier: CA35869258
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs1000085183
gnomAD v3: 1-197039108-T-A
gnomAD v4: 1-197039108-T-A
MyVariant Identifiers: chr1:g.197008238T>A (hg19) chr1:g.197039108T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039108T>A , CM000663.2:g.197039108T>A GRCh38
NC_000001.10:g.197008238T>A , CM000663.1:g.197008238T>A GRCh37
NC_000001.9:g.195274861T>A NCBI36
NG_012065.1:g.33160A>T , LRG_550:g.33160A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*270A>T MANE Select ENSP00000356382.2:n.*270A>T
ENST00000649282.1:c.1011A>T ENSP00000497116.1:n.1011A>T
XM_011509283.2:c.*1191A>T XP_011507585.1:n.*1191A>T
XM_011509284.2:c.*1191A>T XP_011507586.1:n.*1191A>T
XM_011509286.2:c.*1191A>T XP_011507588.1:n.*1191A>T
NM_001994.3:c.*270A>T MANE Select NP_001985.2:n.*270A>T
Search 100 bp 5'
Search 100 bp 3'