Canonical Allele Identifier: CA2062459002

Linked Data

dbSNP Id: rs1884758902

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573553T>A , CM000674.2:g.109573553T>A GRCh38
NC_000012.11:g.110011358T>A , CM000674.1:g.110011358T>A GRCh37
NC_000012.10:g.108495741T>A NCBI36
NG_007096.1:g.4945A>T
NG_007702.1:g.4859T>A , LRG_156:g.4859T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000546277.6:c.-33T>A (MVK) ENSP00000438153.2:n.-33T>A
ENST00000535044.1:n.213T>A (MVK)
ENST00000537236.2:c.-73A>T (MMAB) ENSP00000483818.1:n.-73A>T
ENST00000539335.5:c.-24T>A (MVK) ENSP00000440379.1:n.-24T>A
ENST00000545712.6:c.-73A>T (MMAB) ENSP00000445920.1:n.-73A>T
ENST00000546277.5:c.-33T>A (MVK) ENSP00000438153.1:n.-33T>A
NM_052845.3:c.-73A>T (MMAB) NP_443077.1:n.-73A>T
NR_038118.1:n.1A>T (MMAB)
XM_011538372.1:c.-33T>A (MVK) XP_011536674.1:n.-33T>A
XM_017019313.2:c.-33T>A (MVK) XP_016874802.1:n.-33T>A
XM_024448961.1:c.-73A>T (MMAB) XP_024304729.1:n.-73A>T
XM_024448982.1:c.-33T>A (MVK) XP_024304750.1:n.-33T>A