LDH info

Canonical Allele Identifier: CA11276122
Gene: NPAS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1811399

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100862552C>A , CM000664.2:g.100862552C>A GRCh38
NC_000002.11:g.101479014C>A , CM000664.1:g.101479014C>A GRCh37
NC_000002.10:g.100845446C>A NCBI36
NG_023259.1:g.47402C>A

Transcript Alleles

HGVS Amino-acid change
NM_002518.3:c.-23+42138C>A VV NP_002509.2:p.=
XM_005263953.1:c.173+41353C>A XP_005264010.1:p.=
XM_005263954.1:c.173+41353C>A XP_005264011.1:p.=
XM_005263957.1:c.173+41353C>A XP_005264014.1:p.=
XM_005263959.1:c.173+41353C>A XP_005264016.1:p.=
XM_005263960.1:c.173+41353C>A XP_005264017.1:p.=
XM_011511242.1:c.-23+42138C>A XP_011509544.1:p.=
XM_011511243.1:c.173+41353C>A XP_011509545.1:p.=
XR_922928.1:n.175+41353C>A
XM_005263953.2:c.173+41353C>A XP_005264010.1:p.=
XM_005263959.2:c.173+41353C>A XP_005264016.1:p.=
XM_005263960.2:c.173+41353C>A XP_005264017.1:p.=
XM_011511242.2:c.-23+42138C>A XP_011509544.1:p.=
XM_011511243.2:c.173+41353C>A XP_011509545.1:p.=
XM_017004214.1:c.173+41353C>A XP_016859703.1:p.=
XM_017004215.1:c.173+41353C>A XP_016859704.1:p.=
XM_017004216.1:c.173+41353C>A XP_016859705.1:p.=
XM_017004217.1:c.173+41353C>A XP_016859706.1:p.=
NM_002518.4:c.-23+42138C>A VV MANE Preferred NP_002509.2:p.=
ENST00000335681.9:c.-23+42138C>A ENSP00000338283.5:p.=
ENST00000427413.5:c.173+41353C>A ENSP00000397595.2:p.=