Canonical Allele Identifier: CA527346887

Gene: FASLG

Linked Data

• dbSNP Id: rs1276223879
• gnomAD v2: 1-172633278-A-C
• gnomAD v3: 1-172664138-A-C
• gnomAD v4: 1-172664138-A-C
• MyVariant Identifiers: chr1:g.172633278A>C (hg19) ; chr1:g.172664138A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172664138A>C , CM000663.2:g.172664138A>C	GRCh38
NC_000001.10:g.172633278A>C , CM000663.1:g.172633278A>C	GRCh37
NC_000001.9:g.170899901A>C	NCBI36
NG_007269.1:g.10094A>C , LRG_58:g.10094A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.395-196A>C MANE Select	ENSP00000356694.2:n.395-196A>C
ENST00000340030.4:c.349-196A>C	ENSP00000344739.3:n.349-196A>C
ENST00000367721.2:c.395-196A>C	ENSP00000356694.2:n.395-196A>C
NM_000639.2:c.395-196A>C	NP_000630.1:n.395-196A>C
NM_001302746.1:c.349-196A>C	NP_001289675.1:n.349-196A>C
NM_000639.3:c.395-196A>C MANE Select	NP_000630.1:n.395-196A>C
NM_001302746.2:c.349-196A>C	NP_001289675.1:n.349-196A>C