Canonical Allele Identifier: CA133891492
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs901630163
MyVariant Identifiers: chr6:g.6145209T>C (hg19) chr6:g.6144976T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6144976T>C , CM000668.2:g.6144976T>C GRCh38
NC_000006.11:g.6145209T>C , CM000668.1:g.6145209T>C GRCh37
NC_000006.10:g.6090208T>C NCBI36
NG_008107.1:g.180716A>G , LRG_549:g.180716A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.*643A>G MANE Select ENSP00000264870.3:n.*643A>G
ENST00000264870.7:c.*643A>G ENSP00000264870.3:n.*643A>G
NM_000129.3:c.*643A>G , LRG_549t1:c.*643A>G NP_000120.2:n.*643A>G
XM_006715010.2:c.*643A>G XP_006715073.1:n.*643A>G
XM_011514342.1:c.*643A>G XP_011512644.1:n.*643A>G
NM_000129.4:c.*643A>G MANE Select NP_000120.2:n.*643A>G
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