Canonical Allele Identifier: CA362739907
Gene: F13A1 HGNC NCBI

Linked Data

gnomAD v4: 6-6224711-C-T
MyVariant Identifiers: chr6:g.6224944C>T (hg19) chr6:g.6224711C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224711C>T , CM000668.2:g.6224711C>T GRCh38
NC_000006.11:g.6224944C>T , CM000668.1:g.6224944C>T GRCh37
NC_000006.10:g.6169943C>T NCBI36
NG_008107.1:g.100981G>A , LRG_549:g.100981G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.948G>A MANE Select ENSP00000264870.3:p.Trp316Ter
ENST00000264870.7:c.948G>A ENSP00000264870.3:p.Trp316Ter
ENST00000445223.1:c.98G>A
NM_000129.3:c.948G>A , LRG_549t1:c.948G>A NP_000120.2:p.Trp316Ter
XM_006715010.2:c.948G>A XP_006715073.1:p.Trp316Ter
XM_011514342.1:c.1110G>A XP_011512644.1:p.Trp370Ter
NM_000129.4:c.948G>A MANE Select NP_000120.2:p.Trp316Ter
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