Canonical Allele Identifier: CA414899359
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124365G>C (hg19) chrX:g.154896090G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896090G>C , CM000685.2:g.154896090G>C GRCh38
NC_000023.10:g.154124365G>C , CM000685.1:g.154124365G>C GRCh37
NC_000023.9:g.153777559G>C NCBI36
NG_011403.1:g.131634C>G
NG_011403.2:g.131634C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6416C>G MANE Select ENSP00000353393.4:p.Thr2139Ser
ENST00000360256.8:c.6416C>G ENSP00000353393.4:p.Thr2139Ser
NM_000132.3:c.6416C>G NP_000123.1:p.Thr2139Ser
XM_011531126.1:c.6311C>G XP_011529428.1:p.Thr2104Ser
NM_000132.4:c.6416C>G MANE Select NP_000123.1:p.Thr2139Ser
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Search 100 bp 3'