Canonical Allele Identifier: CA362739861
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6224924T>C (hg19) chr6:g.6224691T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6224691T>C , CM000668.2:g.6224691T>C GRCh38
NC_000006.11:g.6224924T>C , CM000668.1:g.6224924T>C GRCh37
NC_000006.10:g.6169923T>C NCBI36
NG_008107.1:g.101001A>G , LRG_549:g.101001A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.968A>G MANE Select ENSP00000264870.3:p.Asn323Ser
ENST00000264870.7:c.968A>G ENSP00000264870.3:p.Asn323Ser
ENST00000445223.1:c.118A>G
NM_000129.3:c.968A>G , LRG_549t1:c.968A>G NP_000120.2:p.Asn323Ser
XM_006715010.2:c.968A>G XP_006715073.1:p.Asn323Ser
XM_011514342.1:c.1130A>G XP_011512644.1:p.Asn377Ser
NM_000129.4:c.968A>G MANE Select NP_000120.2:p.Asn323Ser
Search 100 bp 5'
Search 100 bp 3'