Canonical Allele Identifier: CA448498822
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6167751G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6167518G>T , CM000668.2:g.6167518G>T GRCh38
NC_000006.11:g.6167751G>T , CM000668.1:g.6167751G>T GRCh37
NC_000006.10:g.6112750G>T NCBI36
NG_008107.1:g.158174C>A , LRG_549:g.158174C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.1848C>A MANE Select ENSP00000264870.3:p.Thr616=
ENST00000264870.7:c.1848C>A ENSP00000264870.3:p.Thr616=
NM_000129.3:c.1848C>A , LRG_549t1:c.1848C>A NP_000120.2:p.Thr616=
XM_006715010.2:c.1848C>A XP_006715073.1:p.Thr616=
XM_011514342.1:c.2010C>A XP_011512644.1:p.Thr670=
NM_000129.4:c.1848C>A MANE Select NP_000120.2:p.Thr616=
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