Canonical Allele Identifier: CA448645848
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6225016G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224783G>T , CM000668.2:g.6224783G>T GRCh38
NC_000006.11:g.6225016G>T , CM000668.1:g.6225016G>T GRCh37
NC_000006.10:g.6170015G>T NCBI36
NG_008107.1:g.100909C>A , LRG_549:g.100909C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.876C>A MANE Select ENSP00000264870.3:p.Ala292=
ENST00000264870.7:c.876C>A ENSP00000264870.3:p.Ala292=
ENST00000445223.1:c.26C>A
NM_000129.3:c.876C>A , LRG_549t1:c.876C>A NP_000120.2:p.Ala292=
XM_006715010.2:c.876C>A XP_006715073.1:p.Ala292=
XM_011514342.1:c.1038C>A XP_011512644.1:p.Ala346=
NM_000129.4:c.876C>A MANE Select NP_000120.2:p.Ala292=
Search 100 bp 5'
Search 100 bp 3'