Canonical Allele Identifier: CA362737681
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6182355T>C (hg19) chr6:g.6182122T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6182122T>C , CM000668.2:g.6182122T>C GRCh38
NC_000006.11:g.6182355T>C , CM000668.1:g.6182355T>C GRCh37
NC_000006.10:g.6127354T>C NCBI36
NG_008107.1:g.143570A>G , LRG_549:g.143570A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.1325A>G MANE Select ENSP00000264870.3:p.Tyr442Cys
ENST00000264870.7:c.1325A>G ENSP00000264870.3:p.Tyr442Cys
NM_000129.3:c.1325A>G , LRG_549t1:c.1325A>G NP_000120.2:p.Tyr442Cys
XM_006715010.2:c.1325A>G XP_006715073.1:p.Tyr442Cys
XM_011514342.1:c.1487A>G XP_011512644.1:p.Tyr496Cys
NM_000129.4:c.1325A>G MANE Select NP_000120.2:p.Tyr442Cys
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