Canonical Allele Identifier: CA448645879

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6225067G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224834G>C , CM000668.2:g.6224834G>C	GRCh38
NC_000006.11:g.6225067G>C , CM000668.1:g.6225067G>C	GRCh37
NC_000006.10:g.6170066G>C	NCBI36
NG_008107.1:g.100858C>G , LRG_549:g.100858C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.825C>G MANE Select	ENSP00000264870.3:p.Val275=
ENST00000264870.7:c.825C>G	ENSP00000264870.3:p.Val275=
NM_000129.3:c.825C>G , LRG_549t1:c.825C>G	NP_000120.2:p.Val275=
XM_006715010.2:c.825C>G	XP_006715073.1:p.Val275=
XM_011514342.1:c.987C>G	XP_011512644.1:p.Val329=
NM_000129.4:c.825C>G MANE Select	NP_000120.2:p.Val275=