Canonical Allele Identifier: CA82071823

Gene: LSAMP

Linked Data

• dbSNP Id: rs1039234597
• gnomAD v2: 3-116181084-T-C
• gnomAD v3: 3-116462237-T-C
• gnomAD v4: 3-116462237-T-C
• MyVariant Identifiers: chr3:g.116181084T>C (hg19) ; chr3:g.116462237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462237T>C , CM000665.2:g.116462237T>C	GRCh38
NC_000003.11:g.116181084T>C , CM000665.1:g.116181084T>C	GRCh37
NC_000003.10:g.117663774T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17282A>G	ENSP00000418506.1:n.179-17282A>G