Canonical Allele Identifier: CA1395153753
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs2049673723

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116462129A>C , CM000665.2:g.116462129A>C GRCh38
NC_000003.11:g.116180976A>C , CM000665.1:g.116180976A>C GRCh37
NC_000003.10:g.117663666A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.179-17174T>G ENSP00000418506.1:n.179-17174T>G