Canonical Allele Identifier: CA2621468982

Linked Data

dbSNP Id: rs2137633285

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121857449C>A , CM000674.2:g.121857449C>A GRCh38
NC_000012.11:g.122295355C>A , CM000674.1:g.122295355C>A GRCh37
NC_000012.10:g.120779738C>A NCBI36
NG_016461.1:g.36163G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289004.8:c.94-17G>T (HPD) MANE Select ENSP00000289004.4:n.94-17G>T
ENST00000535114.1:n.433G>T (HPD)
ENST00000542159.2:n.135G>T (HPD)
ENST00000543163.5:c.-24-17G>T (HPD) ENSP00000441677.1:n.-24-17G>T
NM_001171993.1:c.-24-17G>T (HPD) NP_001165464.1:n.-24-17G>T
NM_002150.2:c.94-17G>T (HPD) NP_002141.1:n.94-17G>T
XR_002957437.1:n.324-170C>A (TIALD)
NM_002150.3:c.94-17G>T (HPD) MANE Select NP_002141.2:n.94-17G>T
NM_001171993.2:c.-24-17G>T (HPD) NP_001165464.1:n.-24-17G>T