Canonical Allele Identifier: CA343993341
Gene: F13B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.197008543T>G (hg19) chr1:g.197039413T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039413T>G , CM000663.2:g.197039413T>G GRCh38
NC_000001.10:g.197008543T>G , CM000663.1:g.197008543T>G GRCh37
NC_000001.9:g.195275166T>G NCBI36
NG_012065.1:g.32855A>C , LRG_550:g.32855A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367412.2:c.1953-2A>C MANE Select ENSP00000356382.2:n.1953-2A>C
ENST00000649282.1:c.708-2A>C ENSP00000497116.1:n.708-2A>C
ENST00000367412.1:c.1953-2A>C ENSP00000356382.1:n.1953-2A>C
NM_001994.2:c.1953-2A>C , LRG_550t1:c.1953-2A>C NP_001985.2:n.1953-2A>C
XM_011509283.2:c.*886A>C XP_011507585.1:n.*886A>C
XM_011509284.2:c.*886A>C XP_011507586.1:n.*886A>C
XM_011509286.2:c.*886A>C XP_011507588.1:n.*886A>C
NM_001994.3:c.1953-2A>C MANE Select NP_001985.2:n.1953-2A>C
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