Canonical Allele Identifier: CA357246827

Gene: ALB

Linked Data

• COSMIC: COSM3826181
• MyVariant Identifiers: chr4:g.74285358T>C (hg19) ; chr4:g.73419641T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419641T>C , CM000666.2:g.73419641T>C	GRCh38
NC_000004.11:g.74285358T>C , CM000666.1:g.74285358T>C	GRCh37
NC_000004.10:g.74504222T>C	NCBI36
NG_009291.1:g.20387T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1785+2T>C MANE Select	ENSP00000295897.4:n.1785+2T>C
ENST00000295897.8:c.1785+2T>C	ENSP00000295897.4:n.1785+2T>C
ENST00000401494.7:c.1440+2T>C	ENSP00000384695.3:n.1440+2T>C
ENST00000415165.6:c.1209+2T>C	ENSP00000401820.2:n.1209+2T>C
ENST00000476441.6:c.*1064+2T>C	ENSP00000423727.1:n.*1064+2T>C
ENST00000495173.1:n.93+2T>C
ENST00000503124.5:c.1335+2T>C	ENSP00000421027.1:n.1335+2T>C
ENST00000505649.5:n.1332+2T>C
ENST00000508932.5:n.175+186T>C
ENST00000509063.5:c.1785+2T>C	ENSP00000422784.1:n.1785+2T>C
ENST00000511370.1:c.1318+2T>C
ENST00000621085.4:c.1146+2T>C	ENSP00000483421.1:n.1146+2T>C
ENST00000621628.4:c.1146+2T>C	ENSP00000480485.1:n.1146+2T>C
NM_000477.5:c.1785+2T>C	NP_000468.1:n.1785+2T>C
NM_000477.6:c.1785+2T>C	NP_000468.1:n.1785+2T>C
NM_000477.7:c.1785+2T>C MANE Select	NP_000468.1:n.1785+2T>C