Canonical Allele Identifier: CA362740046
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6225009C>A (hg19) chr6:g.6224776C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224776C>A , CM000668.2:g.6224776C>A GRCh38
NC_000006.11:g.6225009C>A , CM000668.1:g.6225009C>A GRCh37
NC_000006.10:g.6170008C>A NCBI36
NG_008107.1:g.100916G>T , LRG_549:g.100916G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.883G>T MANE Select ENSP00000264870.3:p.Gly295Ter
ENST00000264870.7:c.883G>T ENSP00000264870.3:p.Gly295Ter
ENST00000445223.1:c.33G>T
NM_000129.3:c.883G>T , LRG_549t1:c.883G>T NP_000120.2:p.Gly295Ter
XM_006715010.2:c.883G>T XP_006715073.1:p.Gly295Ter
XM_011514342.1:c.1045G>T XP_011512644.1:p.Gly349Ter
NM_000129.4:c.883G>T MANE Select NP_000120.2:p.Gly295Ter
Search 100 bp 5'
Search 100 bp 3'