Canonical Allele Identifier: CA12179097
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs3024321
gnomAD v2: 6-6318126-A-G
gnomAD v3: 6-6317893-A-G
gnomAD v4: 6-6317893-A-G
MyVariant Identifiers: chr6:g.6318126A>G (hg19) chr6:g.6317893A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6317893A>G , CM000668.2:g.6317893A>G GRCh38
NC_000006.11:g.6318126A>G , CM000668.1:g.6318126A>G GRCh37
NC_000006.10:g.6263125A>G NCBI36
NG_008107.1:g.7799T>C , LRG_549:g.7799T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.130+642T>C MANE Select ENSP00000264870.3:n.130+642T>C
ENST00000264870.7:c.130+642T>C ENSP00000264870.3:n.130+642T>C
ENST00000414279.5:c.130+642T>C ENSP00000413334.1:n.130+642T>C
ENST00000431222.6:c.292+642T>C ENSP00000416295.2:n.292+642T>C
ENST00000451619.1:c.204+642T>C
NM_000129.3:c.130+642T>C , LRG_549t1:c.130+642T>C NP_000120.2:n.130+642T>C
XM_006715010.2:c.130+642T>C XP_006715073.1:n.130+642T>C
XM_011514342.1:c.292+642T>C XP_011512644.1:n.292+642T>C
NM_000129.4:c.130+642T>C MANE Select NP_000120.2:n.130+642T>C
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