Canonical Allele Identifier: CA474558025

Gene: FADS2

Linked Data

• dbSNP Id: rs1272470824
• gnomAD v2: 11-61633095-TC-T
• gnomAD v4: 11-61865623-TC-T
• MyVariant Identifiers: chr11:g.61633096del (hg19) ; chr11:g.61865624del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61865627del , CM000673.2:g.61865627del	GRCh38
NC_000011.9:g.61633099del , CM000673.1:g.61633099del	GRCh37
NC_000011.8:g.61389675del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.1284-11del MANE Select	ENSP00000278840.4:n.1284-11del
ENST00000257261.10:c.1218-11del	ENSP00000257261.6:n.1218-11del
ENST00000278840.8:c.1284-11del	ENSP00000278840.4:n.1284-11del
ENST00000522056.5:c.1191-11del	ENSP00000429500.1:n.1191-11del
ENST00000523235.5:n.3364-11del
NM_001281501.1:c.1218-11del	NP_001268430.1:n.1218-11del
NM_001281502.1:c.1191-11del	NP_001268431.1:n.1191-11del
NM_004265.3:c.1284-11del	NP_004256.1:n.1284-11del
NM_004265.4:c.1284-11del MANE Select	NP_004256.1:n.1284-11del