Canonical Allele Identifier: CA133891824
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs751314413
gnomAD v2: 6-6145592-T-C
gnomAD v3: 6-6145359-T-C
gnomAD v4: 6-6145359-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145359T>C , CM000668.2:g.6145359T>C GRCh38
NC_000006.11:g.6145592T>C , CM000668.1:g.6145592T>C GRCh37
NC_000006.10:g.6090591T>C NCBI36
NG_008107.1:g.180333A>G , LRG_549:g.180333A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*260A>G MANE Select ENSP00000264870.3:n.*260A>G
ENST00000264870.7:c.*260A>G ENSP00000264870.3:n.*260A>G
NM_000129.3:c.*260A>G , LRG_549t1:c.*260A>G NP_000120.2:n.*260A>G
XM_006715010.2:c.*260A>G XP_006715073.1:n.*260A>G
XM_011514342.1:c.*260A>G XP_011512644.1:n.*260A>G
NM_000129.4:c.*260A>G MANE Select NP_000120.2:n.*260A>G