Canonical Allele Identifier: CA11909185
Gene:

Linked Data

dbSNP Id: rs11730243

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542556C>T , CM000666.2:g.105542556C>T GRCh38
NC_000004.11:g.106463713C>T , CM000666.1:g.106463713C>T GRCh37
NC_000004.10:g.106683162C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.449G>A
XR_939039.1:n.609G>A
XR_939040.1:n.296-1080G>A
XR_001741410.1:n.464G>A
XR_001741411.1:n.940G>A
XR_001741412.1:n.449+15G>A
XR_001741413.1:n.464G>A
XR_001741414.1:n.449+15G>A
XR_939038.2:n.464G>A
XR_939040.2:n.311-1080G>A