Canonical Allele Identifier: CA134398171
Gene: F13A1 HGNC NCBI

Linked Data

dbSNP Id: rs989171980
MyVariant Identifiers: chr6:g.6286074C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6286074C>G , CM000668.2:g.6286074C>G GRCh38
NC_000006.11:g.6286307C>G , CM000668.1:g.6286307C>G GRCh37
NC_000006.10:g.6231306C>G NCBI36
NG_008107.1:g.39618G>C , LRG_549:g.39618G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.320-19265G>C MANE Select ENSP00000264870.3:n.320-19265G>C
ENST00000264870.7:c.320-19265G>C ENSP00000264870.3:n.320-19265G>C
ENST00000414279.5:c.320-19265G>C ENSP00000413334.1:n.320-19265G>C
ENST00000431222.6:c.482-19265G>C ENSP00000416295.2:n.482-19265G>C
ENST00000479211.1:n.305-19265G>C
NM_000129.3:c.320-19265G>C , LRG_549t1:c.320-19265G>C NP_000120.2:n.320-19265G>C
XM_006715010.2:c.320-19265G>C XP_006715073.1:n.320-19265G>C
XM_011514342.1:c.482-19265G>C XP_011512644.1:n.482-19265G>C
NM_000129.4:c.320-19265G>C MANE Select NP_000120.2:n.320-19265G>C
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