Canonical Allele Identifier: CA2677189020
Gene: F13A1 HGNC NCBI

Linked Data

gnomAD v4: 6-6145022-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145022C>G , CM000668.2:g.6145022C>G GRCh38
NC_000006.11:g.6145255C>G , CM000668.1:g.6145255C>G GRCh37
NC_000006.10:g.6090254C>G NCBI36
NG_008107.1:g.180670G>C , LRG_549:g.180670G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*597G>C MANE Select ENSP00000264870.3:n.*597G>C
ENST00000264870.7:c.*597G>C ENSP00000264870.3:n.*597G>C
NM_000129.3:c.*597G>C , LRG_549t1:c.*597G>C NP_000120.2:n.*597G>C
XM_006715010.2:c.*597G>C XP_006715073.1:n.*597G>C
XM_011514342.1:c.*597G>C XP_011512644.1:n.*597G>C
NM_000129.4:c.*597G>C MANE Select NP_000120.2:n.*597G>C
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