Canonical Allele Identifier: CA362738908
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs121913070
gnomAD v4: 6-6195859-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6195859C>T , CM000668.2:g.6195859C>T GRCh38
NC_000006.11:g.6196092C>T , CM000668.1:g.6196092C>T GRCh37
NC_000006.10:g.6141091C>T NCBI36
NG_008107.1:g.129833G>A , LRG_549:g.129833G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.1243G>A MANE Select ENSP00000264870.3:p.Val415Ile
ENST00000264870.7:c.1243G>A ENSP00000264870.3:p.Val415Ile
NM_000129.3:c.1243G>A , LRG_549t1:c.1243G>A NP_000120.2:p.Val415Ile
XM_006715010.2:c.1243G>A XP_006715073.1:p.Val415Ile
XM_011514342.1:c.1405G>A XP_011512644.1:p.Val469Ile
NM_000129.4:c.1243G>A MANE Select NP_000120.2:p.Val415Ile