Canonical Allele Identifier: CA362655866
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs1417549782
gnomAD v3: 6-6145644-T-C
gnomAD v4: 6-6145644-T-C
MyVariant Identifiers: chr6:g.6145877T>C (hg19) chr6:g.6145644T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145644T>C , CM000668.2:g.6145644T>C GRCh38
NC_000006.11:g.6145877T>C , CM000668.1:g.6145877T>C GRCh37
NC_000006.10:g.6090876T>C NCBI36
NG_008107.1:g.180048A>G , LRG_549:g.180048A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.2174A>G MANE Select ENSP00000264870.3:p.Gln725Arg
ENST00000264870.7:c.2174A>G ENSP00000264870.3:p.Gln725Arg
NM_000129.3:c.2174A>G , LRG_549t1:c.2174A>G NP_000120.2:p.Gln725Arg
XM_006715010.2:c.2174A>G XP_006715073.1:p.Gln725Arg
XM_011514342.1:c.2336A>G XP_011512644.1:p.Gln779Arg
NM_000129.4:c.2174A>G MANE Select NP_000120.2:p.Gln725Arg
Search 100 bp 5'
Search 100 bp 3'