Canonical Allele Identifier: CA2591318639
Gene: F13A1 HGNC NCBI

Linked Data

gnomAD v3: 6-6145051-G-C
gnomAD v4: 6-6145051-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145051G>C , CM000668.2:g.6145051G>C GRCh38
NC_000006.11:g.6145284G>C , CM000668.1:g.6145284G>C GRCh37
NC_000006.10:g.6090283G>C NCBI36
NG_008107.1:g.180641C>G , LRG_549:g.180641C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*568C>G MANE Select ENSP00000264870.3:n.*568C>G
ENST00000264870.7:c.*568C>G ENSP00000264870.3:n.*568C>G
NM_000129.3:c.*568C>G , LRG_549t1:c.*568C>G NP_000120.2:n.*568C>G
XM_006715010.2:c.*568C>G XP_006715073.1:n.*568C>G
XM_011514342.1:c.*568C>G XP_011512644.1:n.*568C>G
NM_000129.4:c.*568C>G MANE Select NP_000120.2:n.*568C>G
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