Canonical Allele Identifier: CA133891616

Gene: F13A1

Linked Data

• dbSNP Id: rs751133183
• MyVariant Identifiers: chr6:g.6145320G>A (hg19) ; chr6:g.6145087G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145087G>A , CM000668.2:g.6145087G>A	GRCh38
NC_000006.11:g.6145320G>A , CM000668.1:g.6145320G>A	GRCh37
NC_000006.10:g.6090319G>A	NCBI36
NG_008107.1:g.180605C>T , LRG_549:g.180605C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*532C>T MANE Select	ENSP00000264870.3:n.*532C>T
ENST00000264870.7:c.*532C>T	ENSP00000264870.3:n.*532C>T
NM_000129.3:c.*532C>T , LRG_549t1:c.*532C>T	NP_000120.2:n.*532C>T
XM_006715010.2:c.*532C>T	XP_006715073.1:n.*532C>T
XM_011514342.1:c.*532C>T	XP_011512644.1:n.*532C>T
NM_000129.4:c.*532C>T MANE Select	NP_000120.2:n.*532C>T