Canonical Allele Identifier: CA421944410
Gene: FASLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.172634787T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665647T>G , CM000663.2:g.172665647T>G GRCh38
NC_000001.10:g.172634787T>G , CM000663.1:g.172634787T>G GRCh37
NC_000001.9:g.170901410T>G NCBI36
NG_007269.1:g.11603T>G , LRG_58:g.11603T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367721.3:c.477T>G MANE Select ENSP00000356694.2:p.Pro159=
ENST00000340030.4:c.*47T>G ENSP00000344739.3:n.*47T>G
ENST00000367721.2:c.477T>G ENSP00000356694.2:p.Pro159=
NM_000639.2:c.477T>G NP_000630.1:p.Pro159=
NM_001302746.1:c.*47T>G NP_001289675.1:n.*47T>G
NM_000639.3:c.477T>G MANE Select NP_000630.1:p.Pro159=
NM_001302746.2:c.*47T>G NP_001289675.1:n.*47T>G
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