Canonical Allele Identifier: CA35869334
Gene: F13B HGNC NCBI

Linked Data

dbSNP Id: rs974185748
MyVariant Identifiers: chr1:g.197008448A>T (hg19) chr1:g.197039318A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039318A>T , CM000663.2:g.197039318A>T GRCh38
NC_000001.10:g.197008448A>T , CM000663.1:g.197008448A>T GRCh37
NC_000001.9:g.195275071A>T NCBI36
NG_012065.1:g.32950T>A , LRG_550:g.32950T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.*60T>A MANE Select ENSP00000356382.2:n.*60T>A
ENST00000649282.1:c.801T>A ENSP00000497116.1:n.801T>A
ENST00000367412.1:c.*60T>A ENSP00000356382.1:n.*60T>A
NM_001994.2:c.*60T>A , LRG_550t1:c.*60T>A NP_001985.2:n.*60T>A
XM_011509283.2:c.*981T>A XP_011507585.1:n.*981T>A
XM_011509284.2:c.*981T>A XP_011507586.1:n.*981T>A
XM_011509286.2:c.*981T>A XP_011507588.1:n.*981T>A
NM_001994.3:c.*60T>A MANE Select NP_001985.2:n.*60T>A
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