Canonical Allele Identifier: CA362740279
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6248562G>C (hg19) chr6:g.6248329G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6248329G>C , CM000668.2:g.6248329G>C GRCh38
NC_000006.11:g.6248562G>C , CM000668.1:g.6248562G>C GRCh37
NC_000006.10:g.6193561G>C NCBI36
NG_008107.1:g.77363C>G , LRG_549:g.77363C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.781C>G MANE Select ENSP00000264870.3:p.Arg261Gly
ENST00000264870.7:c.781C>G ENSP00000264870.3:p.Arg261Gly
NM_000129.3:c.781C>G , LRG_549t1:c.781C>G NP_000120.2:p.Arg261Gly
XM_006715010.2:c.781C>G XP_006715073.1:p.Arg261Gly
XM_011514342.1:c.943C>G XP_011512644.1:p.Arg315Gly
NM_000129.4:c.781C>G MANE Select NP_000120.2:p.Arg261Gly
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