Canonical Allele Identifier: CA1482797961
Gene:

Linked Data

dbSNP Id: rs1724787484

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542881G>C , CM000666.2:g.105542881G>C GRCh38
NC_000004.11:g.106464038G>C , CM000666.1:g.106464038G>C GRCh37
NC_000004.10:g.106683487G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-172C>G
XR_939039.1:n.456-172C>G
XR_939040.1:n.296-1405C>G
XR_001741410.1:n.311-172C>G
XR_001741411.1:n.787-172C>G
XR_001741412.1:n.311-172C>G
XR_001741413.1:n.311-172C>G
XR_001741414.1:n.311-172C>G
XR_939038.2:n.311-172C>G
XR_939040.2:n.311-1405C>G