Canonical Allele Identifier: CA103381280
Gene:

Linked Data

dbSNP Id: rs887509024

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542491G>A , CM000666.2:g.105542491G>A GRCh38
NC_000004.11:g.106463648G>A , CM000666.1:g.106463648G>A GRCh37
NC_000004.10:g.106683097G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.514C>T
XR_939039.1:n.674C>T
XR_939040.1:n.296-1015C>T
XR_001741410.1:n.529C>T
XR_001741411.1:n.1005C>T
XR_001741412.1:n.449+80C>T
XR_001741413.1:n.529C>T
XR_001741414.1:n.449+80C>T
XR_939038.2:n.529C>T
XR_939040.2:n.311-1015C>T