LDH info

Canonical Allele Identifier: CA164948049
Gene: CFTR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1013075

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478856T>C , CM000669.2:g.117478856T>C GRCh38
NC_000007.13:g.117118910T>C , CM000669.1:g.117118910T>C GRCh37
NC_000007.12:g.116906146T>C NCBI36
NG_016465.4:g.18073T>C , LRG_663:g.18073T>C

Transcript Alleles

HGVS Amino-acid change
XM_011515751.1:c.42-388T>C XP_011514053.1:p.=
XM_011515752.1:c.42-388T>C XP_011514054.1:p.=
XM_011515754.1:c.-1241T>C XP_011514056.1:p.=
ENST00000546407.1:n.166+3048T>C