Canonical Allele Identifier: CA133891896

Gene: F13A1

Linked Data

• dbSNP Id: rs755670896
• gnomAD v4: 6-6145437-G-C
• MyVariant Identifiers: chr6:g.6145670G>C (hg19) ; chr6:g.6145437G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145437G>C , CM000668.2:g.6145437G>C	GRCh38
NC_000006.11:g.6145670G>C , CM000668.1:g.6145670G>C	GRCh37
NC_000006.10:g.6090669G>C	NCBI36
NG_008107.1:g.180255C>G , LRG_549:g.180255C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*182C>G MANE Select	ENSP00000264870.3:n.*182C>G
ENST00000264870.7:c.*182C>G	ENSP00000264870.3:n.*182C>G
NM_000129.3:c.*182C>G , LRG_549t1:c.*182C>G	NP_000120.2:n.*182C>G
XM_006715010.2:c.*182C>G	XP_006715073.1:n.*182C>G
XM_011514342.1:c.*182C>G	XP_011512644.1:n.*182C>G
NM_000129.4:c.*182C>G MANE Select	NP_000120.2:n.*182C>G