Canonical Allele Identifier: CA1607973352
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs1583059013
gnomAD v4: 6-6181933-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6181933A>G , CM000668.2:g.6181933A>G GRCh38
NC_000006.11:g.6182166A>G , CM000668.1:g.6182166A>G GRCh37
NC_000006.10:g.6127165A>G NCBI36
NG_008107.1:g.143759T>C , LRG_549:g.143759T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.1459+55T>C MANE Select ENSP00000264870.3:n.1459+55T>C
ENST00000264870.7:c.1459+55T>C ENSP00000264870.3:n.1459+55T>C
NM_000129.3:c.1459+55T>C , LRG_549t1:c.1459+55T>C NP_000120.2:n.1459+55T>C
XM_006715010.2:c.1459+55T>C XP_006715073.1:n.1459+55T>C
XM_011514342.1:c.1621+55T>C XP_011512644.1:n.1621+55T>C
NM_000129.4:c.1459+55T>C MANE Select NP_000120.2:n.1459+55T>C
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