Canonical Allele Identifier: CA362737688
Gene: F13A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.6182357A>C (hg19) chr6:g.6182124A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6182124A>C , CM000668.2:g.6182124A>C GRCh38
NC_000006.11:g.6182357A>C , CM000668.1:g.6182357A>C GRCh37
NC_000006.10:g.6127356A>C NCBI36
NG_008107.1:g.143568T>G , LRG_549:g.143568T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.1323T>G MANE Select ENSP00000264870.3:p.Ile441Met
ENST00000264870.7:c.1323T>G ENSP00000264870.3:p.Ile441Met
NM_000129.3:c.1323T>G , LRG_549t1:c.1323T>G NP_000120.2:p.Ile441Met
XM_006715010.2:c.1323T>G XP_006715073.1:p.Ile441Met
XM_011514342.1:c.1485T>G XP_011512644.1:p.Ile495Met
NM_000129.4:c.1323T>G MANE Select NP_000120.2:p.Ile441Met
Search 100 bp 5'
Search 100 bp 3'