Canonical Allele Identifier: CA648328371
Gene: LSAMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061194G>C , CM000665.2:g.117061194G>C GRCh38
NC_000003.11:g.116780041G>C , CM000665.1:g.116780041G>C GRCh37
NC_000003.10:g.118262731G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474851.1:c.34-51820C>G ENSP00000418506.1:n.34-51820C>G