Canonical Allele Identifier: CA15952408

Linked Data

dbSNP Id: rs4803457

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41355454T>C , CM000681.2:g.41355454T>C GRCh38
NC_000019.9:g.41861359T>C , CM000681.1:g.41861359T>C GRCh37
NC_000019.8:g.46553199T>C NCBI36
NG_013091.1:g.13720A>G
NG_013364.1:g.3473A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243578.8:c.215-441A>G (B9D2) MANE Select ENSP00000243578.2:n.215-441A>G
ENST00000675972.1:c.215-441A>G (B9D2) ENSP00000501911.1:n.215-441A>G
ENST00000243578.7:c.215-441A>G (B9D2) ENSP00000243578.2:n.215-441A>G
ENST00000539627.5:c.-30+4252T>C (TMEM91) ENSP00000441900.1:n.-30+4252T>C
ENST00000594416.1:c.*61-441A>G (B9D2) ENSP00000469666.1:n.*61-441A>G
ENST00000604123.5:c.142+1139T>C (TMEM91) ENSP00000474871.1:n.142+1139T>C
ENST00000604424.1:n.350+4252T>C
NM_030578.3:c.215-441A>G (B9D2) NP_085055.2:n.215-441A>G
XM_006723405.1:c.89-441A>G (B9D2) XP_006723468.1:n.89-441A>G
XM_011527349.1:c.215-441A>G (B9D2) XP_011525651.1:n.215-441A>G
XM_011527350.1:c.56-441A>G (B9D2) XP_011525652.1:n.56-441A>G
XM_011527349.2:c.215-441A>G (B9D2) XP_011525651.1:n.215-441A>G
XM_011527350.2:c.56-441A>G (B9D2) XP_011525652.1:n.56-441A>G
NM_030578.4:c.215-441A>G (B9D2) MANE Select NP_085055.2:n.215-441A>G