Canonical Allele Identifier: CA82071820

Gene: LSAMP

Linked Data

• dbSNP Id: rs912049111
• gnomAD v3: 3-116462225-G-C
• gnomAD v4: 3-116462225-G-C
• MyVariant Identifiers: chr3:g.116181072G>C (hg19) ; chr3:g.116462225G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116462225G>C , CM000665.2:g.116462225G>C	GRCh38
NC_000003.11:g.116181072G>C , CM000665.1:g.116181072G>C	GRCh37
NC_000003.10:g.117663762G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474851.1:c.179-17270C>G	ENSP00000418506.1:n.179-17270C>G