Canonical Allele Identifier: CA2580073396

Gene: MAP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.72107531G>C , CM000667.2:g.72107531G>C	GRCh38
NC_000005.9:g.71403358G>C , CM000667.1:g.71403358G>C	GRCh37
NC_000005.8:g.71439114G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005909.5:c.-1G>C MANE Select	NP_005900.2:n.-1G>C
ENST00000296755.12:c.-1G>C MANE Select	ENSP00000296755.7:n.-1G>C
NM_005909.3:c.-1G>C	NP_005900.2:n.-1G>C
NM_005909.4:c.-1G>C	NP_005900.2:n.-1G>C
ENST00000296755.11:c.-1G>C	ENSP00000296755.7:n.-1G>C
ENST00000504183.1:n.55G>C
ENST00000511641.2:c.-1G>C	ENSP00000423444.2:n.-1G>C
ENST00000512974.5:c.-1G>C	ENSP00000426312.1:n.-1G>C
ENST00000513526.6:c.-1G>C	ENSP00000427194.2:n.-1G>C
XR_001742725.2:n.699+394C>G
XR_001742726.1:n.168+394C>G
XR_001742727.2:n.2735+1244C>G
XR_001742729.2:n.2798+394C>G
XR_001742730.2:n.699+394C>G
XR_001742731.2:n.699+394C>G
XR_001742732.2:n.699+394C>G
XR_001742734.2:n.699+394C>G
XR_001742735.1:n.168+394C>G
XR_001742736.2:n.699+394C>G
XR_001742737.2:n.699+394C>G
XR_001742738.2:n.699+394C>G
XR_001742739.1:n.168+394C>G
XR_001742740.2:n.699+394C>G
XR_001742741.1:n.168+394C>G
XR_948462.1:n.680+394C>G
XR_948464.1:n.180+1244C>G
XR_948465.1:n.7C>G
XR_948466.1:n.243+394C>G
XR_948468.1:n.7C>G