Canonical Allele Identifier: CA1395448056
Gene: LSAMP HGNC NCBI

Linked Data

dbSNP Id: rs1708215756

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061112T>C , CM000665.2:g.117061112T>C GRCh38
NC_000003.11:g.116779959T>C , CM000665.1:g.116779959T>C GRCh37
NC_000003.10:g.118262649T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.34-51738A>G ENSP00000418506.1:n.34-51738A>G