Canonical Allele Identifier: CA362661781
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6174959A>C (hg19) chr6:g.6174726A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6174726A>C , CM000668.2:g.6174726A>C GRCh38
NC_000006.11:g.6174959A>C , CM000668.1:g.6174959A>C GRCh37
NC_000006.10:g.6119958A>C NCBI36
NG_008107.1:g.150966T>G , LRG_549:g.150966T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.1601T>G MANE Select ENSP00000264870.3:p.Phe534Cys
ENST00000264870.7:c.1601T>G ENSP00000264870.3:p.Phe534Cys
NM_000129.3:c.1601T>G , LRG_549t1:c.1601T>G NP_000120.2:p.Phe534Cys
XM_006715010.2:c.1601T>G XP_006715073.1:p.Phe534Cys
XM_011514342.1:c.1763T>G XP_011512644.1:p.Phe588Cys
NM_000129.4:c.1601T>G MANE Select NP_000120.2:p.Phe534Cys
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